Clearance Summary
LIFECARE COMPACT TENS DEVICE received FDA 510(k) clearance under submission number K003369, sponsored by Lifecare , Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2001-03-08.
- Submission: K003369
- Applicant / Sponsor: Lifecare , Ltd.
- Clearance pathway: Traditional
- Review panel: Neurology
- Device class: Class II
- Regulation citation: 21 CFR 882.5890
- Decision date: 2001-03-08
Classification & Regulation
This clearance is catalogued under FDA product code GZJ and 21 CFR 882.5890, within the Neurology review panel as a Class II device.