Clearance Summary
PHYSIOGLOVE ES received FDA 510(k) clearance under submission number K050674, sponsored by Commwell , Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2006-04-25.
- Submission: K050674
- Applicant / Sponsor: Commwell , Ltd.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2340
- Decision date: 2006-04-25
Classification & Regulation
This clearance is catalogued under FDA product code DPS and 21 CFR 870.2340, within the Cardiovascular review panel as a Class II device.