ELECSYS CK-MB STAT
K-Number: K974421 · 1997-12-17
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Device Summary
Frequently Asked Questions
What is the ELECSYS CK-MB STAT?
ELECSYS CK-MB STAT is a medical device that received FDA 510(k) clearance on 1997-12-17. The listed applicant is Boehringer Mannheim Corp.. The 510(k) number is K974421.
When did ELECSYS CK-MB STAT receive FDA 510(k) clearance?
ELECSYS CK-MB STAT received FDA 510(k) clearance on 1997-12-17, under 510(k) number K974421.
Who is the listed applicant for ELECSYS CK-MB STAT?
The FDA 510(k) record lists Boehringer Mannheim Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ELECSYS CK-MB STAT?
The FDA product code for ELECSYS CK-MB STAT is JHY.
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 Boehringer Mannheim Corp. 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: JHY)
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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