meddevicedb.com FDA Device Reference

STORZ ULTRA-SOURCE HIGH OUTPUT ILLUMINATOR

K904616 Class II Traditional
Decision Date
1991-04-19
Sponsor / Applicant
Storz Instrument Co.

Technical Specification

510(k) Submission ID K904616
Product Code HBI
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4580
Decision Date 1991-04-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

STORZ ULTRA-SOURCE HIGH OUTPUT ILLUMINATOR received FDA 510(k) clearance under submission number K904616, sponsored by Storz Instrument Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1991-04-19.

Classification & Regulation

This clearance is catalogued under FDA product code HBI and 21 CFR 878.4580, within the General, Plastic Surgery review panel as a Class II device.