Clearance Summary
ABPM MOBIL-O-GRAPH BLOOD PRESSURE MONITOR, MODEL ABP CONTROL received FDA 510(k) clearance under submission number K964235, sponsored by Industrielle Entwicklung Medizintechnik Und Vertri. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1999-03-02.
- Submission: K964235
- Applicant / Sponsor: Industrielle Entwicklung Medizintechnik Und Vertri
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1130
- Decision date: 1999-03-02
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.