Clearance Summary
ANGIO-PRESS LITE DVT Compression Device received FDA 510(k) clearance under submission number K173012, sponsored by Pegasus Medical Supply, 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 2018-05-10.
- Submission: K173012
- Applicant / Sponsor: Pegasus Medical Supply, Inc.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.5800
- Decision date: 2018-05-10
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.