CREATINE KINASE TEST (CK) ITEM NUMBER 65411— 510(k) K903333

Name: FDA 510(k) clearance K903333
Creator: U.S. Food and Drug Administration
Published: 1990-08-17

Substantially Equivalent

Em Diagnostic Systems, Inc.

FDA 510(k) clearance K903333 for CREATINE KINASE TEST (CK) ITEM NUMBER 65411, Substantially Equivalent on 1990-08-17. Applicant: Em Diagnostic Systems, Inc.. Device class: 2.

Clearance details

Applicant: Em Diagnostic Systems, Inc.
Product code: Code CGS
Device class: Class 2
Regulation: 21 CFR 862.1215
Advisory panel: Clinical Chemistry
Date received: 1990-07-25
Decision date: 1990-08-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Gibbstown, NJ, US

Download summary PDF View on FDA.gov ↗

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