AURA TEK FDP— 510(k) K970353

Substantially Equivalent

Perimmune, Inc.

FDA 510(k) clearance K970353 for AURA TEK FDP, Substantially Equivalent on 1997-04-30. Applicant: Perimmune, Inc..

Clearance details

Applicant: Perimmune, Inc.
Product code: Code MMW
Advisory panel: Immunology
Date received: 1997-01-30
Decision date: 1997-04-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rockville, MD, US

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