IN VITRO DIAGNOSTIC REAGENT— 510(k) K772096

Substantially Equivalent

Pcl-Ria, Inc.

FDA 510(k) clearance K772096 for IN VITRO DIAGNOSTIC REAGENT, Substantially Equivalent on 1977-11-22. Applicant: Pcl-Ria, Inc..

Clearance details

Applicant: Pcl-Ria, Inc.
Product code: Code CDX
Advisory panel: Clinical Chemistry
Date received: 1977-11-07
Decision date: 1977-11-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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