BRACHEAL-LARGE VESSEL CLIP
K-Number: K780288 · 1978-02-28
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Device Summary
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.
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
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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