meddevicedb.com FDA Device Reference

SLIT LAMP, MODELS HS-5000, HS-5500 AND HS-7500

K093639 Class II Traditional
Decision Date
2009-12-03
Sponsor / Applicant
Huvitz Co., Ltd.

Technical Specification

510(k) Submission ID K093639
Product Code HJO
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.1850
Decision Date 2009-12-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SLIT LAMP, MODELS HS-5000, HS-5500 AND HS-7500 received FDA 510(k) clearance under submission number K093639, sponsored by Huvitz Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 2009-12-03.

Classification & Regulation

This clearance is catalogued under FDA product code HJO and 21 CFR 886.1850, within the Ophthalmic review panel as a Class II device.