Clearance Summary
ULTRASOUND SCANNER, TYPE 2102 received FDA 510(k) clearance under submission number K011417, sponsored by B-K Medical A/S. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2001-06-08.
- Submission: K011417
- Applicant / Sponsor: B-K Medical A/S
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.1560
- Decision date: 2001-06-08
Classification & Regulation
This clearance is catalogued under FDA product code IYO and 21 CFR 892.1560, within the Radiology review panel as a Class II device.