Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

G-PROX EZ ENDOSCOPIC GRASPER

K-Number: K103688 · 2011-01-14

ApplicantUsgi Medical
Decision Date2011-01-14
Product CodeOCZ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

G-PROX EZ 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 2011-01-14 under 510(k) number K103688. The device is classified under product code OCZ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the G-PROX EZ ENDOSCOPIC GRASPER?

G-PROX EZ ENDOSCOPIC GRASPER is a medical device that received FDA 510(k) clearance on 2011-01-14. The listed applicant is Usgi Medical. The 510(k) number is K103688.

When did G-PROX EZ ENDOSCOPIC GRASPER receive FDA 510(k) clearance?

G-PROX EZ ENDOSCOPIC GRASPER received FDA 510(k) clearance on 2011-01-14, under 510(k) number K103688.

Who is the listed applicant for G-PROX EZ 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 EZ ENDOSCOPIC GRASPER?

The FDA product code for G-PROX EZ ENDOSCOPIC GRASPER is OCZ.

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: OCZ)

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.

↑