REAGENT, ALKALINE PHOSPHATASE DETERM.— 510(k) K760474

Name: FDA 510(k) clearance K760474
Creator: U.S. Food and Drug Administration
Published: 1976-10-29

Substantially Equivalent

Simmler & Son, Inc.

FDA 510(k) clearance K760474 for REAGENT, ALKALINE PHOSPHATASE DETERM., Substantially Equivalent on 1976-10-29. Applicant: Simmler & Son, Inc.. Device class: 2.

Clearance details

Applicant: Simmler & Son, Inc.
Product code: Code CJE
Device class: Class 2
Regulation: 21 CFR 862.1050
Advisory panel: Clinical Chemistry
Date received: 1976-08-17
Decision date: 1976-10-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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