K-ASSAY FIBRINOGEN— 510(k) K993482

Substantially Equivalent

Kamiya Biomedical Co.

FDA 510(k) clearance K993482 for K-ASSAY FIBRINOGEN, Substantially Equivalent on 1999-12-06. Applicant: Kamiya Biomedical Co..

Clearance details

Applicant: Kamiya Biomedical Co.
Product code: Code GIS
Advisory panel: Hematology
Date received: 1999-10-14
Decision date: 1999-12-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Seattle, WA, US

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