PARA-PAK CLEAN VIAL— 510(k) K792710

Substantially Equivalent

Meridian Diagnostics, Inc.

FDA 510(k) clearance K792710 for PARA-PAK CLEAN VIAL, Substantially Equivalent on 1980-01-28. Applicant: Meridian Diagnostics, Inc..

Clearance details

Applicant: Meridian Diagnostics, Inc.
Product code: Code FMH
Advisory panel: Pathology
Date received: 1979-12-27
Decision date: 1980-01-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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