PARA-PAK PLUS— 510(k) K931770

Substantially Equivalent

Meridian Diagnostics, Inc.

FDA 510(k) clearance K931770 for PARA-PAK PLUS, Substantially Equivalent on 1993-06-15. Applicant: Meridian Diagnostics, Inc..

Clearance details

Applicant: Meridian Diagnostics, Inc.
Product code: Code LIO
Advisory panel: Microbiology
Date received: 1993-04-09
Decision date: 1993-06-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Cincinnati, OH, US

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