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K-ASSAY® Plasma Control

KAMIYA BIOMEDICAL COMPANY, LLC · Model K81C-6M · UDI-DI 00816426020894

GGC Prescription
10
510(k) clearances
1
Adverse events
0
Recalls
21
Facilities

Description

For use as a consistent test sample of known concentration for monitoring assay conditions for the listed constituents.

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.