K-ASSAY CRP— 510(k) K991224

Substantially Equivalent

Kamiya Biomedical Co.

FDA 510(k) clearance K991224 for K-ASSAY CRP, Substantially Equivalent on 1999-05-14. Applicant: Kamiya Biomedical Co..

Clearance details

Applicant: Kamiya Biomedical Co.
Product code: Code DCK
Advisory panel: Immunology
Date received: 1999-04-12
Decision date: 1999-05-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Seattle, WA, US

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