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FDA 510(k)

BRACHEAL-LARGE VESSEL CLIP

K-Number: K780288 · 1978-02-28

Decision Date1978-02-28
Product CodeGDJ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BRACHEAL-LARGE VESSEL 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 1978-02-28 under 510(k) number K780288. The device is classified under product code GDJ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BRACHEAL-LARGE VESSEL CLIP?

BRACHEAL-LARGE VESSEL CLIP is a medical device that received FDA 510(k) clearance on 1978-02-28. The listed applicant is Edward Weck, Inc.. The 510(k) number is K780288.

When did BRACHEAL-LARGE VESSEL CLIP receive FDA 510(k) clearance?

BRACHEAL-LARGE VESSEL CLIP received FDA 510(k) clearance on 1978-02-28, under 510(k) number K780288.

Who is the listed applicant for BRACHEAL-LARGE VESSEL 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 BRACHEAL-LARGE VESSEL CLIP?

The FDA product code for BRACHEAL-LARGE VESSEL CLIP is GDJ.

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: GDJ)

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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