UNICLIP SURGICAL CLIP APPLIER
K-Number: K926199 · 1993-04-20
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Device Summary
Frequently Asked Questions
What is the UNICLIP SURGICAL CLIP APPLIER?
UNICLIP SURGICAL CLIP APPLIER is a medical device that received FDA 510(k) clearance on 1993-04-20. The listed applicant is Unisurge, Inc.. The 510(k) number is K926199.
When did UNICLIP SURGICAL CLIP APPLIER receive FDA 510(k) clearance?
UNICLIP SURGICAL CLIP APPLIER received FDA 510(k) clearance on 1993-04-20, under 510(k) number K926199.
Who is the listed applicant for UNICLIP SURGICAL CLIP APPLIER?
The FDA 510(k) record lists Unisurge, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for UNICLIP SURGICAL CLIP APPLIER?
The FDA product code for UNICLIP SURGICAL CLIP APPLIER is GDO.
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 Unisurge, 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: GDO)
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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