Clearance Summary
RECOVER ADULT VEIN WARMER received FDA 510(k) clearance under submission number K963689, sponsored by Florida Medical Industries, 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 1996-12-12.
- Submission: K963689
- Applicant / Sponsor: Florida Medical Industries, Inc.
- Clearance pathway: Traditional
- Review panel: Physical Medicine
- Device class: Class I
- Regulation citation: 21 CFR 890.5710
- Decision date: 1996-12-12
Classification & Regulation
This clearance is catalogued under FDA product code IMD and 21 CFR 890.5710, within the Physical Medicine review panel as a Class I device.