meddevicedb.com FDA Device Reference

GRASPING FORCEPS

K914110 Class II Traditional
Decision Date
1992-02-28
Sponsor / Applicant
Annex Medical, Inc.

Technical Specification

510(k) Submission ID K914110
Product Code FGO
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.4680
Decision Date 1992-02-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

GRASPING FORCEPS received FDA 510(k) clearance under submission number K914110, sponsored by Annex Medical, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 1992-02-28.

Classification & Regulation

This clearance is catalogued under FDA product code FGO and 21 CFR 876.4680, within the Gastroenterology, Urology review panel as a Class II device.