meddevicedb.com FDA Device Reference

DAVOL LAPAROSCOPIC DISSECTORS

K920234 Class II Traditional
Decision Date
1993-02-05
Sponsor / Applicant
C.R. Bard, Inc.

Technical Specification

510(k) Submission ID K920234
Product Code HET
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.1720
Decision Date 1993-02-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DAVOL LAPAROSCOPIC DISSECTORS received FDA 510(k) clearance under submission number K920234, sponsored by C.R. Bard, 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 1993-02-05.

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.