meddevicedb.com FDA Device Reference

ENDOPATH DISPOSABLE SURGICAL TROCAR REDUCER

K904907 Class II Traditional
Decision Date
1991-01-24
Sponsor / Applicant
ETHICON, Inc.

Technical Specification

510(k) Submission ID K904907
Product Code HET
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.1720
Decision Date 1991-01-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ENDOPATH DISPOSABLE SURGICAL TROCAR REDUCER received FDA 510(k) clearance under submission number K904907, sponsored by ETHICON, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Obstetrics/Gynecology review panel. The statutory decision date of record is 1991-01-24.

Classification & Regulation

This clearance is catalogued under FDA product code HET and 21 CFR 884.1720, within the Obstetrics/Gynecology review panel as a Class II device.