meddevicedb.com FDA Device Reference

STETSON/S.LOREN/LH.BAZAAR/G.VANDERBILT/P.BALMAIN

K933423 Class I Traditional
Decision Date
1993-09-20
Sponsor / Applicant
Thunder Industries, Inc.

Technical Specification

510(k) Submission ID K933423
Product Code HQZ
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.5842
Decision Date 1993-09-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

STETSON/S.LOREN/LH.BAZAAR/G.VANDERBILT/P.BALMAIN received FDA 510(k) clearance under submission number K933423, sponsored by Thunder Industries, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 1993-09-20.

Classification & Regulation

This clearance is catalogued under FDA product code HQZ and 21 CFR 886.5842, within the Ophthalmic review panel as a Class I device.