meddevicedb.com FDA Device Reference

FLEXIBLE TROCAR TUBES

K930215 Class II Traditional
Decision Date
1993-03-16
Sponsor / Applicant
Olympus Corp.

Technical Specification

510(k) Submission ID K930215
Product Code EWY
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.4720
Decision Date 1993-03-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FLEXIBLE TROCAR TUBES received FDA 510(k) clearance under submission number K930215, sponsored by Olympus Corp.. 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 1993-03-16.

Classification & Regulation

This clearance is catalogued under FDA product code EWY and 21 CFR 874.4720, within the Ear, Nose, Throat review panel as a Class II device.