Clearance Summary
BIOFLEX LD-175 AND LD-1200 TREATMENT HEADS received FDA 510(k) clearance under submission number K041885, sponsored by Meditech International, Inc.. 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 2005-02-24.
- Submission: K041885
- Applicant / Sponsor: Meditech International, Inc.
- Clearance pathway: Traditional
- Review panel: Physical Medicine
- Device class: Class II
- Regulation citation: 21 CFR 890.5500
- Decision date: 2005-02-24
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.