meddevicedb.com FDA Device Reference

SCALAR WAVE LASER SYSTEM

K091158 Class II Traditional
Decision Date
2009-08-10
Sponsor / Applicant
Stellar Lasers

Technical Specification

510(k) Submission ID K091158
Product Code ILY
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5500
Decision Date 2009-08-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SCALAR WAVE LASER SYSTEM received FDA 510(k) clearance under submission number K091158, sponsored by Stellar Lasers. The device was reviewed via the Traditional premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 2009-08-10.

Classification & Regulation

This clearance is catalogued under FDA product code ILY and 21 CFR 890.5500, within the Physical Medicine review panel as a Class II device.