Clearance Summary
REPROCESSED COMPRESSION LIMB SLEEVES received FDA 510(k) clearance under submission number K012658, sponsored by Surgical Instruments Service and Savings, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2002-05-14.
- Submission: K012658
- Applicant / Sponsor: Surgical Instruments Service and Savings, Inc.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.5800
- Decision date: 2002-05-14
Classification & Regulation
This clearance is catalogued under FDA product code JOW and 21 CFR 870.5800, within the Cardiovascular review panel as a Class II device.