COSGROVE CLAMP
K-Number: K974769 · 1998-06-12
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Device Summary
Frequently Asked Questions
What is the COSGROVE CLAMP?
COSGROVE CLAMP is a medical device that received FDA 510(k) clearance on 1998-06-12. The listed applicant is Allegiance Healthcare Corp.. The 510(k) number is K974769.
When did COSGROVE CLAMP receive FDA 510(k) clearance?
COSGROVE CLAMP received FDA 510(k) clearance on 1998-06-12, under 510(k) number K974769.
Who is the listed applicant for COSGROVE CLAMP?
The FDA 510(k) record lists Allegiance Healthcare Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for COSGROVE CLAMP?
The FDA product code for COSGROVE CLAMP is DXC.
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 Allegiance Healthcare 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: DXC)
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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