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FDA 510(k)

HEM-O-LOK LIGATION CLIP

K-Number: K062914 · 2006-11-02

Decision Date2006-11-02
Product CodeFZP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

HEM-O-LOK LIGATION CLIP is the device name listed in this FDA 510(k) record. The listed applicant is Teleflex Medical. It received FDA 510(k) clearance on 2006-11-02 under 510(k) number K062914. 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 HEM-O-LOK LIGATION CLIP?

HEM-O-LOK LIGATION CLIP is a medical device that received FDA 510(k) clearance on 2006-11-02. The listed applicant is Teleflex Medical. The 510(k) number is K062914.

When did HEM-O-LOK LIGATION CLIP receive FDA 510(k) clearance?

HEM-O-LOK LIGATION CLIP received FDA 510(k) clearance on 2006-11-02, under 510(k) number K062914.

Who is the listed applicant for HEM-O-LOK LIGATION CLIP?

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

What is the FDA product code for HEM-O-LOK LIGATION CLIP?

The FDA product code for HEM-O-LOK LIGATION 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 Teleflex Medical 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 40 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

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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