Clearance Summary
NORELCO ANEROID BLOOD PRESSURE METER received FDA 510(k) clearance under submission number K811634, sponsored by North American Philips Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1981-06-30.
- Submission: K811634
- Applicant / Sponsor: North American Philips Corp.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1120
- Decision date: 1981-06-30
Classification & Regulation
This clearance is catalogued under FDA product code DXQ and 21 CFR 870.1120, within the Cardiovascular review panel as a Class II device.