Scantibodies Laboratory, Inc.

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Web: http://www.scantibodies.com
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Address: 9336 Abraham Way, Santee, California 92017, USA
Phone: +1-(619)-258-9300 | Fax: +1-(619)-258-9366 | Map/Directions >>

Profile: Scantibodies Laboratory, Inc. delivers diagnostic products. Our product line comprises of antibodies, blockers, controls, kits and plasma/serum.

FDA Registration Number: 2020808

19 Products/Services (Click for related suppliers)

• ACTH Radioimmunoassay Test (FDA Code: CKG / 862.1025)

An adrenocorticotropic hormone (ACTH) test system is a device intended to measure adrenocorticotropic hormone in plasma and serum. ACTH measurements are used in the differential diagnosis and treatment of certain disorders of the adrenal glands such as Cushing's syndrome, adrenocortical insufficiency, and the ectopic ACTH syndrome.

• Bio-Intact PTH Testing Kit

• Calcitonin

• Calcitonin Assay Immunoradiometric (IRMA) Assay

• Calcitonin ELISA Kit

• Calcitonin Immunoassay

• calcitonin nasal Spray

• Calcitonin Radioimmunoassay

• Calcitonin Radioimmunoassay Test (FDA Code: JKR / 862.1140)

A calcitonin test system is a device intended to measure the thyroid hormone calcitonin (thyrocalcitonin) levels in plasma and serum. Calcitonin measurements are used in the diagnosis and treatment of diseases involving the thyroid and parathyroid glands, including carcinoma and hyperparathyroidism (excessive activity of the parathyroid gland).

• Calcitonin RIA Kit

• HCG Over The Counter Pregnancy Test Kit (FDA Code: LCX / 862.1155)

A human chorionic gonadotropin (HCG) test system is a device intended for the early detection of pregnancy is intended to measure HCG, a placental hormone, in plasma or urine.

• Intact PTH

• Luteinizing Hormone Radioimmunoassay (FDA Code: CEP / 862.1485)

A luteinizing hormone test system is a device intended to measure luteinizing hormone in serum and urine. Luteinizing hormone measurements are used in the diagnosis and treatment of gonadal dysfunction.

• Multi Analyte Control (FDA Code: JJY / 862.1660)

A quality control material (assayed and unassayed) for clinical chemistry is a device intended for medical purposes for use in a test system to estimate test precision and to detect systematic analytical deviations that may arise from reagent or analytical instrument variation. A quality control material (assayed and unassayed) may be used for proficiency testing in interlaboratory surveys. This generic type of device includes controls (assayed and unassayed) for blood gases, electrolytes, enzymes, multianalytes (all kinds), single (specified) analytes, or urinalysis controls.

• Mycobacterium Tuberculosis Cell-Mediated Immunity Test (FDA Code: NCD)

• Over The Counter Luteinizing Hormone (Lh) Test (FDA Code: NGE / 862.1485)

• Parathyroid Hormone Radioimmunoassay Test (FDA Code: CEW / 862.1545)

A parathyroid hormone test system is a device intended to measure the levels of parathyroid hormone in serum and plasma. Measurements of parathyroid hormone levels are used in the differential diagnosis of hypercalcemia (abnormally high levels of calcium in the blood) and hypocalcemia (abnormally low levels of calcium in the blood) resulting from disorders of calcium metabolism.

• Primary Calibrator (FDA Code: JIS / 862.1150)

A calibrator is a device intended for medical purposes for use in a test system to establish points of reference that are used in the determination of values in the measurement of substances in human specimens. (See also 862.2 in this part.)

• Thyroid Stimulating Hormone Radioimmunoassay (FDA Code: JLW / 862.1690)

A thyroid stimulating hormone test system is a device intended to measure thyroid stimulating hormone, also known as thyrotrophin and thyrotrophic hormone, in serum and plasma. Measurements of thyroid stimulating hormone produced by the anterior pituitary are used in the diagnosis of thyroid or pituitary disorders.