VISUWELL GROUP A STREPTOCOCCUS DETECTION KIT— 510(k) K890840

Substantially Equivalent

Adi Diagnostics, Inc.

FDA 510(k) clearance K890840 for VISUWELL GROUP A STREPTOCOCCUS DETECTION KIT, Substantially Equivalent on 1989-03-27. Applicant: Adi Diagnostics, Inc..

Clearance details

Applicant: Adi Diagnostics, Inc.
Product code: Code GTZ
Advisory panel: Microbiology
Date received: 1989-02-21
Decision date: 1989-03-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rexdale, Ontario, CA

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