Pulse Scientific, Inc.

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Contact: Allen Chan - President
Web: http://www.pulsescientific.com
E-Mail:
Address: 5100 S. Service Rd., Unit 18, Burlington, Ontario L7L 6A5, Canada
Phone: +1-(905)-333-8188 | Fax: +1-(905)-333-0500 | Map/Directions >>

Profile: Pulse Scientific, Inc. specializes in medical diagnostic products. Our three main product categories are latex test kits, febrile antigen, and rapid diagnostic tests. Our urine reagent strips are plastic strips to which are affixed seperate reagent areas. They provide tests for the semi-quantitative determinators of pH, protein, glucose, ketone, bilirubin, blood, nitrite, and urobilinogen in urine. The test results may provide information regarding the status of carbohydrate metabolism, kidney function, liver function, acid-base balance, and bacteriurea.

The company was founded in 1992, has revenues of USD 1-5 Million, has ~10 employees and is ISO 13485 certified.

FDA Registration Number: 8044007
US Agent: Allen Chan / Pulse Scientific Corp.
Phone: +1-(716)-433-0056 Fax: +1-(716)-433-0058 E-Mail:

10 Products/Services (Click for related suppliers)

• Anti-Streptokinase Test (FDA Code: GTO / 866.3720)

• C-Reactive Protein (CRP), FITC Conjugate (FDA Code: DCK / 866.5270)

A C-reactive protein immunological test system is a device that consists of the reagents used to measure by immunochemical techniques the C-reactive protein in serum and other body fluids. Measurement of C-reactive protein aids in evaluation of the amount of injury to body tissues.

• C-Reactive Protein Test System (FDA Code: DCN / 866.5270)

• 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.

• Human Chorionic Gonadotropin Agglutination Method (FDA Code: JHJ / 862.1155)

• Human Chorionic Gonadotropin Radioimmunoassay (FDA Code: JHI / 862.1155)

• Infectious Mononucleosis Test System (FDA Code: KTN / 866.5640)

An infectious mononucleosis immunological test system is a device that consists of the reagents used to measure by immunochemical techniques heterophile antibodies frequently associated with infectious mononucleosis in serum, plasma, and other body fluids. Measurements of these antibodies aid in the diagnosis of infectious mononucleosis.

• Non-Treponemal Antigen (FDA Code: GMQ / 866.3820)

• Rheumatoid Factor Test System (FDA Code: DHR / 866.5775)

A rheumatoid factor immunological test system is a device that consists of the reagents used to measure by immunochemical techniques the rheumatoid factor (antibodies to immunoglobulins) in serum, other body fluids, and tissues. Measurement of rheumatoid factor may aid in the diagnosis of rheumatoid arthritis.

• Systemic Lupus Erythematosus Test (FDA Code: DHC / 866.5820)

A systemic lupus erythematosus (SLE) immunological test system is a device that consists of the reagents used to measure by immunochemical techniques the autoimmune antibodies in serum and other body fluids that react with cellular nuclear double-stranded deoxyribonucleic acid (DNA) or other nuclear constituents that are specifically diagnostic of SLE. Measurement of nuclear double-stranded DNA antibodies aids in the diagnosis of SLE (a multisystem autoimmune disease in which tissues are attacked by the person's own antibodies).