EMDS CREATINE KINASE ITEM NIMBER 65411
K-Number: K893691 · 1989-08-31
Advertisement
Device Summary
Frequently Asked Questions
What is the EMDS CREATINE KINASE ITEM NIMBER 65411?
EMDS CREATINE KINASE ITEM NIMBER 65411 is a medical device that received FDA 510(k) clearance on 1989-08-31. The listed applicant is Diagnostic Systems. The 510(k) number is K893691.
When did EMDS CREATINE KINASE ITEM NIMBER 65411 receive FDA 510(k) clearance?
EMDS CREATINE KINASE ITEM NIMBER 65411 received FDA 510(k) clearance on 1989-08-31, under 510(k) number K893691.
Who is the listed applicant for EMDS CREATINE KINASE ITEM NIMBER 65411?
The FDA 510(k) record lists Diagnostic Systems as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EMDS CREATINE KINASE ITEM NIMBER 65411?
The FDA product code for EMDS CREATINE KINASE ITEM NIMBER 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 Diagnostic Systems 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.
Advertisement