Clearance Summary
PROCARE MONITOR B20 received FDA 510(k) clearance under submission number K122253, sponsored by Ge Medical Systems China Co., Ltd.. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2013-03-22.
- Submission: K122253
- Applicant / Sponsor: Ge Medical Systems China Co., Ltd.
- Clearance pathway: Special
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1025
- Decision date: 2013-03-22
Classification & Regulation
This clearance is catalogued under FDA product code MHX and 21 CFR 870.1025, within the Cardiovascular review panel as a Class II device.