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FDA 510(k)

COALESCENT SURGICAL U-CLIP - OR OTHER TBD AND ACCESSORIES

K-Number: K021407 · 2002-07-03

Decision Date2002-07-03
Product CodeFZP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

COALESCENT SURGICAL U-CLIP - OR OTHER TBD AND ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Coalescent Surgical. It received FDA 510(k) clearance on 2002-07-03 under 510(k) number K021407. The device is classified under product code FZP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COALESCENT SURGICAL U-CLIP - OR OTHER TBD AND ACCESSORIES?

COALESCENT SURGICAL U-CLIP - OR OTHER TBD AND ACCESSORIES is a medical device that received FDA 510(k) clearance on 2002-07-03. The listed applicant is Coalescent Surgical. The 510(k) number is K021407.

When did COALESCENT SURGICAL U-CLIP - OR OTHER TBD AND ACCESSORIES receive FDA 510(k) clearance?

COALESCENT SURGICAL U-CLIP - OR OTHER TBD AND ACCESSORIES received FDA 510(k) clearance on 2002-07-03, under 510(k) number K021407.

Who is the listed applicant for COALESCENT SURGICAL U-CLIP - OR OTHER TBD AND ACCESSORIES?

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 - OR OTHER TBD AND ACCESSORIES?

The FDA product code for COALESCENT SURGICAL U-CLIP - OR OTHER TBD AND ACCESSORIES 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.

View all 9 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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