ALKALINE PHOSPHATASE REAGENT SET— 510(k) K812837

Name: FDA 510(k) clearance K812837
Creator: U.S. Food and Drug Administration
Published: 1982-01-29

Substantially Equivalent

Anco Medical Reagents & Assoc.

FDA 510(k) clearance K812837 for ALKALINE PHOSPHATASE REAGENT SET, Substantially Equivalent on 1982-01-29. Applicant: Anco Medical Reagents & Assoc.. Device class: 2.

Clearance details

Applicant: Anco Medical Reagents & Assoc.
Product code: Code CJL
Device class: Class 2
Regulation: 21 CFR 862.1050
Advisory panel: Clinical Chemistry
Date received: 1981-10-09
Decision date: 1982-01-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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