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Address: 12076 Santa Fe Drive, P.O. Box 14428, Lenexa, Kansas 66215, USA
www.remelinc.com |
Send Inquiry |
Phone: +1-(913)-888-0939
FDA Registration: 1031428 Year Established: 1973
Employee Count: ~20
Products: Pregnancy Kits, Cotton Swabs, Home pregnancy test kits, Hcg, Early Pregnancy Testing Kit, Sensitive Pregnancy Tests, Diagnostic Test Kits For Pregnancy, ...
Remel offers a wide range of microbiology products that are used in the clinical, industrial, research and academic laboratories. Our products help diagnose infection quickly and accurately, providing
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Address: 4481 Campus Drive, Kalamazoo, Michigan 49008, USA
www.rallansci.com |
Send Inquiry |
Phone: +1-(269)-544-5600
FDA Registration: 1831638
Products: Slide Stainers, Slide Staining, General Medical Supplies, General Diagnostics, General Urology Supplies, General Disinfectants, ...
Richard-allan Scientific produces a complete portfolio of consumable & supplies for the histology, cytology and hematology lab community. We specialize in performance stains, reagents, paraffin, prefi
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Address: 1330 Thurman St., Lodi, California 95240, USA
www.americanmastertech.com |
Phone: +1-(209)-368-4031, 800-860-4073
FDA Registration: 2939235 Quality: ISO 9001:2008 Certified
Products: Acid Containing Decalcifier Pathology Solution (FDA Code:
KDX), Acid Containing Fixative (FDA Code:
LDW), Acid Fuchsin Stain (FDA Code:
IDF), Albumin Based Adhesive (FDA Code:
KEL), Alcian Blue Stain (FDA Code:
IDA), Alcohol Containing Fixative (FDA Code:
LDZ), ...
American Mastertech Scientific, Inc. manufactures and distributes laboratory products & services for hospitals & laboratories. We focus on serving the fields of biology, cytopathology (cytology), hist
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FDA Code / Regulation: KKS / 864.1850 Dye and chemical solution stains for medical purposes are mixtures of synthetic or natural dyes or nondye chemicals in solutions used in staining cells and tissues for diagnostic histopathology, cytopathology, or hematology.
Classification. Class I (general controls). These devices are exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to the limitations in 864.9. These devices are also exempt from the current good manufacturing practice requirements of the quality system regulation in part 820 of this chapter, with the exception of 820.180, with respect to general requirements concerning records, and 820.198, with respect to complaint files.