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FDA 510(k)

HEMOCLIP SURGICAL OCCLUDING CLIP

K-Number: K800079 · 1980-01-28

Decision Date1980-01-28
Product CodeFZP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

HEMOCLIP SURGICAL OCCLUDING CLIP is the device name listed in this FDA 510(k) record. The listed applicant is Edward Weck, Inc.. It received FDA 510(k) clearance on 1980-01-28 under 510(k) number K800079. 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 HEMOCLIP SURGICAL OCCLUDING CLIP?

HEMOCLIP SURGICAL OCCLUDING CLIP is a medical device that received FDA 510(k) clearance on 1980-01-28. The listed applicant is Edward Weck, Inc.. The 510(k) number is K800079.

When did HEMOCLIP SURGICAL OCCLUDING CLIP receive FDA 510(k) clearance?

HEMOCLIP SURGICAL OCCLUDING CLIP received FDA 510(k) clearance on 1980-01-28, under 510(k) number K800079.

Who is the listed applicant for HEMOCLIP SURGICAL OCCLUDING CLIP?

The FDA 510(k) record lists Edward Weck, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HEMOCLIP SURGICAL OCCLUDING CLIP?

The FDA product code for HEMOCLIP SURGICAL OCCLUDING 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 Edward Weck, Inc. 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 140 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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