meddevicedb.com FDA Device Reference

JARIT SURGICAL INSTRUMENTS

K932456 Class II Traditional
Decision Date
1994-04-21
Sponsor / Applicant
J. Jamner Surgical Instruments, Inc.

Technical Specification

510(k) Submission ID K932456
Product Code KNF
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.4160
Decision Date 1994-04-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

JARIT SURGICAL INSTRUMENTS received FDA 510(k) clearance under submission number K932456, sponsored by J. Jamner Surgical Instruments, 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 1994-04-21.

Classification & Regulation

This clearance is catalogued under FDA product code KNF and 21 CFR 884.4160, within the Obstetrics/Gynecology review panel as a Class II device.