Clearance Summary
PRO FOCUS 2202, PRO FOCUS 2202 UV MODEL: TYPE 2202 received FDA 510(k) clearance under submission number K100919, sponsored by B-K Medical Aps. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2011-12-16.
- Submission: K100919
- Applicant / Sponsor: B-K Medical Aps
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.1550
- Decision date: 2011-12-16
Classification & Regulation
This clearance is catalogued under FDA product code IYN and 21 CFR 892.1550, within the Radiology review panel as a Class II device.