ANTIBODY ASSAY FOR DETECTION OF ADENOVIRUS IN CELL— 510(k) K871229

Substantially Equivalent

Microscan Div. Baxter Healthcare Corp.

FDA 510(k) clearance K871229 for ANTIBODY ASSAY FOR DETECTION OF ADENOVIRUS IN CELL, Substantially Equivalent on 1987-06-26. Applicant: Microscan Div. Baxter Healthcare Corp..

Clearance details

Applicant: Microscan Div. Baxter Healthcare Corp.
Product code: Code GOD
Advisory panel: Microbiology
Date received: 1987-03-27
Decision date: 1987-06-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: West Sacramento, CA, US

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