VESOCCLUDE LIGATING CLIP
K-Number: K091060 · 2009-09-23
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Device Summary
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
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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