CREATINE KINASE TEST
K-Number: K931889 · 1993-07-27
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Device Summary
Frequently Asked Questions
What is the CREATINE KINASE TEST?
CREATINE KINASE TEST is a medical device that received FDA 510(k) clearance on 1993-07-27. The listed applicant is Em Diagnostic Systems, Inc.. The 510(k) number is K931889.
When did CREATINE KINASE TEST receive FDA 510(k) clearance?
CREATINE KINASE TEST received FDA 510(k) clearance on 1993-07-27, under 510(k) number K931889.
Who is the listed applicant for CREATINE KINASE TEST?
The FDA 510(k) record lists Em Diagnostic Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CREATINE KINASE TEST?
The FDA product code for CREATINE KINASE TEST is CGS.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Em Diagnostic Systems, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: CGS)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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