COALESCENT SURGICAL U-CLIP
K-Number: K012317 · 2001-08-31
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Device Summary
Frequently Asked Questions
What is the COALESCENT SURGICAL U-CLIP?
COALESCENT SURGICAL U-CLIP is a medical device that received FDA 510(k) clearance on 2001-08-31. The listed applicant is Coalescent Surgical. The 510(k) number is K012317.
When did COALESCENT SURGICAL U-CLIP receive FDA 510(k) clearance?
COALESCENT SURGICAL U-CLIP received FDA 510(k) clearance on 2001-08-31, under 510(k) number K012317.
Who is the listed applicant for COALESCENT SURGICAL U-CLIP?
The FDA 510(k) record lists Coalescent Surgical as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for COALESCENT SURGICAL U-CLIP?
The FDA product code for COALESCENT SURGICAL U-CLIP is FZP.
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 Coalescent Surgical 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: FZP)
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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