meddevicedb.com FDA Device Reference

OPTICAL FORCEPS

K990561 Class II Traditional
Decision Date
1999-05-14
Sponsor / Applicant
Pilling Weck Surgical

Technical Specification

510(k) Submission ID K990561
Product Code JEK
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.4680
Decision Date 1999-05-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OPTICAL FORCEPS received FDA 510(k) clearance under submission number K990561, sponsored by Pilling Weck Surgical. 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 1999-05-14.

Classification & Regulation

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