Clearance Summary
ProBP 2400 Digital Blood Pressure Device received FDA 510(k) clearance under submission number K152770, sponsored by Microlife Intellectual Property GmbH. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2015-10-21.
- Submission: K152770
- Applicant / Sponsor: Microlife Intellectual Property GmbH
- Clearance pathway: Special
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1130
- Decision date: 2015-10-21
Classification & Regulation
This clearance is catalogued under FDA product code DXN and 21 CFR 870.1130, within the Cardiovascular review panel as a Class II device.