Clearance Summary
PRESSUREWIRE CERTUS, MODELS 12006 AND 12306 received FDA 510(k) clearance under submission number K062769, sponsored by Radi Medical Systems AB. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2006-12-04.
- Submission: K062769
- Applicant / Sponsor: Radi Medical Systems AB
- Clearance pathway: Special
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2870
- Decision date: 2006-12-04
Classification & Regulation
This clearance is catalogued under FDA product code DXO and 21 CFR 870.2870, within the Cardiovascular review panel as a Class II device.