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FDA 510(k)

G-PROX ENDOSCOPIC GRASPER

K-Number: K061276 · 2006-12-06

ApplicantUsgi Medical
Decision Date2006-12-06
Product CodeGAT
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

G-PROX ENDOSCOPIC GRASPER is the device name listed in this FDA 510(k) record. The listed applicant is Usgi Medical. It received FDA 510(k) clearance on 2006-12-06 under 510(k) number K061276. The device is classified under product code GAT. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 11 devices →

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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