Clearance Summary
CARDIOMETER received FDA 510(k) clearance under submission number K780117, sponsored by Med General. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1978-02-03.
- Submission: K780117
- Applicant / Sponsor: Med General
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2300
- Decision date: 1978-02-03
Classification & Regulation
This clearance is catalogued under FDA product code DRT and 21 CFR 870.2300, within the Cardiovascular review panel as a Class II device.