Clearance Summary
OSCILLAIR 3000 LOW AIR LOSS KINETIC THERAPY BED received FDA 510(k) clearance under submission number K923710, sponsored by Progressive Medical Technology, 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 1993-03-22.
- Submission: K923710
- Applicant / Sponsor: Progressive Medical Technology, Inc.
- Clearance pathway: Traditional
- Review panel: Physical Medicine
- Device class: Class II
- Regulation citation: 21 CFR 890.5225
- Decision date: 1993-03-22
Classification & Regulation
This clearance is catalogued under FDA product code IKZ and 21 CFR 890.5225, within the Physical Medicine review panel as a Class II device.