meddevicedb.com FDA Device Reference

CANNULATED BIOPSY FORCEPS

K892687 Class II Traditional
Decision Date
1989-06-21
Sponsor / Applicant
Zinnanti Surgical Instruments, Inc.

Technical Specification

510(k) Submission ID K892687
Product Code EOQ
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.4680
Decision Date 1989-06-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CANNULATED BIOPSY FORCEPS received FDA 510(k) clearance under submission number K892687, sponsored by Zinnanti Surgical Instruments, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ear, Nose, Throat review panel. The statutory decision date of record is 1989-06-21.

Classification & Regulation

This clearance is catalogued under FDA product code EOQ and 21 CFR 874.4680, within the Ear, Nose, Throat review panel as a Class II device.