FIBRINOGEN CALIBRATOR KIT— 510(k) K072304

Substantially Equivalent

Dade Behring, Inc.

FDA 510(k) clearance K072304 for FIBRINOGEN CALIBRATOR KIT, Substantially Equivalent on 2007-09-19. Applicant: Dade Behring, Inc..

Clearance details

Applicant: Dade Behring, Inc.
Product code: Code GFX
Advisory panel: Hematology
Date received: 2007-08-17
Decision date: 2007-09-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Newark, DE, US

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