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FDA 510(k)

VESOCCLUDE LIGATING CLIP

K-Number: K091060 · 2009-09-23

Decision Date2009-09-23
Product CodeFZP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

VESOCCLUDE LIGATING CLIP is the device name listed in this FDA 510(k) record. The listed applicant is Vesocclude Medical, LLC. It received FDA 510(k) clearance on 2009-09-23 under 510(k) number K091060. 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 VESOCCLUDE LIGATING CLIP?

VESOCCLUDE LIGATING CLIP is a medical device that received FDA 510(k) clearance on 2009-09-23. The listed applicant is Vesocclude Medical, LLC. The 510(k) number is K091060.

When did VESOCCLUDE LIGATING CLIP receive FDA 510(k) clearance?

VESOCCLUDE LIGATING CLIP received FDA 510(k) clearance on 2009-09-23, under 510(k) number K091060.

Who is the listed applicant for VESOCCLUDE LIGATING CLIP?

The FDA 510(k) record lists Vesocclude Medical, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VESOCCLUDE LIGATING CLIP?

The FDA product code for VESOCCLUDE LIGATING 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 Vesocclude Medical, LLC 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

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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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