Clearance Summary
BCM-600 MINI-SIX EXTRA LG. FIELD ANGIO received FDA 510(k) clearance under submission number K801950, sponsored by B C Medical , Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1980-10-03.
- Submission: K801950
- Applicant / Sponsor: B C Medical , Ltd.
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.1860
- Decision date: 1980-10-03
Classification & Regulation
This clearance is catalogued under FDA product code KPX and 21 CFR 892.1860, within the Radiology review panel as a Class II device.