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K-ASSAY® Fibrinogen Calibrator

KAMIYA BIOMEDICAL COMPANY, LLC · Model KAI-136C · UDI-DI 00816426021082

GIS Prescription
1
510(k) clearances
68
Adverse events (1 deaths)
0
Recalls
7
Facilities

Description

For the calibration of the K-ASSAY® Fibrinogen assay.

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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.