meddevicedb.com FDA Device Reference

TRISTAR LP TORCAR WITH LOW PROFILE THREADED SLEEVE

K965045 Class II Traditional
Decision Date
1997-05-05
Sponsor / Applicant
Ethicon Endo-Surgery, Inc.

Technical Specification

510(k) Submission ID K965045
Product Code HET
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.1720
Decision Date 1997-05-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TRISTAR LP TORCAR WITH LOW PROFILE THREADED SLEEVE received FDA 510(k) clearance under submission number K965045, sponsored by Ethicon Endo-Surgery, 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 1997-05-05.

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.