|
Address: 370 West 1700 South, Logan, Utah 84321, USA
www.wescor.com |
Send Inquiry |
Phone: +1-(435)-752-6011, 800- 453-2725
FDA Registration: 1717966 Year Established: 1970
Annual Revenues: USD 10-25 Million
Employee Count: ~100
Quality: ISO, CE Certified
Products: Slide Stainers, General Diagnostic Supplies, Programmable Slide Stainers, Hematology Slide Stainer Instruments, Neurology Instruments, General Chemistry Kits, ...
Wescor manufactures & markets instrumentation & other products for medicine, science and industry. Our unique vapor pressure and colloid osmometers, automatic slide stainers, cytocentrifuges & diagnos
more...
|
Address: 5182 West 76th St., Minneapolis, Minnesota 55439, USA
Phone: +1-(952)-646-3168
FDA Registration: 1832816
Products: Blood Lancets, Blood Lancet Needle (Pen Type), Blood Lancet Needle (Blade Type), Stainless Steel Blood Lancets, Plastic Blood Lancets, Blood Collection Lancet (FDA Code:
FMK), ...
Arkray Factory USA, Inc. is engaged in the production of medical and surgical equipments. Our product line includes urine test strips, urine chemistry analyzers, intravascular catheters and blood gluc
more...
|
Address: 202 Hi-Techventure Town, 198-53 Hupyeong-Dong, Chuncheon 200-161, Korea, Republic Of
FDA Registration: 3007301207
Products: Automated Urinalysis System (FDA Code:
KQO), Osmolality Of Serum & Urine Vapor Pressure (FDA Code:
JNA), Urine Leukocyte Test (FDA Code:
LJX), ...
Chungdo Pharm. Co.,Ltd. provides automated urinalysis system, urine leukocyte test, urine test reagent strips and various other medical accessories.
more...
FDA Code / Regulation: JNA / 862.1540 An osmolality test system is a device intended to measure ionic and nonionic solute concentration in body fluids, such as serum and urine. Osmolality measurement is used as an adjunct to other tests in the evaluation of a variety of diseases, including kidney diseases (e.g., chronic progressive renal failure), diabetes insipidus, other endocrine and metabolic disorders, and fluid imbalances.
Classification. Class I (general controls). The device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to 862.9.