Clearance Summary
PeriFlux6000 received FDA 510(k) clearance under submission number K152930, sponsored by Perimed AB. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2016-05-05.
- Submission: K152930
- Applicant / Sponsor: Perimed AB
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2100
- Decision date: 2016-05-05
Classification & Regulation
This clearance is catalogued under FDA product code DPW and 21 CFR 870.2100, within the Cardiovascular review panel as a Class II device.