G-PROX ENDOSCOPIC GRASPER
K-Number: K061276 · 2006-12-06
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Device Summary
Frequently Asked Questions
What is the G-PROX ENDOSCOPIC GRASPER?
G-PROX ENDOSCOPIC GRASPER is a medical device that received FDA 510(k) clearance on 2006-12-06. The listed applicant is Usgi Medical. The 510(k) number is K061276.
When did G-PROX ENDOSCOPIC GRASPER receive FDA 510(k) clearance?
G-PROX ENDOSCOPIC GRASPER received FDA 510(k) clearance on 2006-12-06, under 510(k) number K061276.
Who is the listed applicant for G-PROX ENDOSCOPIC GRASPER?
The FDA 510(k) record lists Usgi Medical as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for G-PROX ENDOSCOPIC GRASPER?
The FDA product code for G-PROX ENDOSCOPIC GRASPER is GAT.
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 Usgi Medical 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: GAT)
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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