Clearance Summary
MLT-1000 IR LASER SYSTEM received FDA 510(k) clearance under submission number K033986, sponsored by Medical Laser Therapeutics LP. 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 2004-03-29.
- Submission: K033986
- Applicant / Sponsor: Medical Laser Therapeutics LP
- Clearance pathway: Traditional
- Review panel: Physical Medicine
- Device class: Class II
- Regulation citation: 21 CFR 890.5500
- Decision date: 2004-03-29
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.