Clearance Summary
G5 APPARATUS T, K1, K3 & THE PRESIDENT MODEL'S received FDA 510(k) clearance under submission number K850851, sponsored by Physio 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 1985-06-25.
- Submission: K850851
- Applicant / Sponsor: Physio Technology, Inc.
- Clearance pathway: Traditional
- Review panel: Physical Medicine
- Device class: Class I
- Regulation citation: 21 CFR 890.5660
- Decision date: 1985-06-25
Classification & Regulation
This clearance is catalogued under FDA product code ISA and 21 CFR 890.5660, within the Physical Medicine review panel as a Class I device.