ULNAR-RADIAL CLIP
K-Number: K780290 · 1978-02-28
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Device Summary
Frequently Asked Questions
What is the ULNAR-RADIAL CLIP?
ULNAR-RADIAL 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 K780290.
When did ULNAR-RADIAL CLIP receive FDA 510(k) clearance?
ULNAR-RADIAL CLIP received FDA 510(k) clearance on 1978-02-28, under 510(k) number K780290.
Who is the listed applicant for ULNAR-RADIAL 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 ULNAR-RADIAL CLIP?
The FDA product code for ULNAR-RADIAL 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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