meddevicedb.com FDA Device Reference

PSL CLASSIC SLIT LAMP

K100500 Class II Traditional
Decision Date
2010-03-09
Sponsor / Applicant
Keeler Instruments, Inc.

Technical Specification

510(k) Submission ID K100500
Product Code HJO
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.1850
Decision Date 2010-03-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PSL CLASSIC SLIT LAMP received FDA 510(k) clearance under submission number K100500, sponsored by Keeler Instruments, 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 2010-03-09.

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.