CREATINE KINASE (CK) TEST ITEM #65411
K-Number: K924704 · 1992-10-13
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Device Summary
Frequently Asked Questions
What is the CREATINE KINASE (CK) TEST ITEM #65411?
CREATINE KINASE (CK) TEST ITEM #65411 is a medical device that received FDA 510(k) clearance on 1992-10-13. The listed applicant is Em Diagnostic Systems, Inc.. The 510(k) number is K924704.
When did CREATINE KINASE (CK) TEST ITEM #65411 receive FDA 510(k) clearance?
CREATINE KINASE (CK) TEST ITEM #65411 received FDA 510(k) clearance on 1992-10-13, under 510(k) number K924704.
Who is the listed applicant for CREATINE KINASE (CK) TEST ITEM #65411?
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 (CK) TEST ITEM #65411?
The FDA product code for CREATINE KINASE (CK) TEST ITEM #65411 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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