Clearance Summary
DISP. TRANSDUCER DOMES TD200 & TD300 received FDA 510(k) clearance under submission number K802069, sponsored by Bio-Med 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 1980-09-09.
- Submission: K802069
- Applicant / Sponsor: Bio-Med Corp.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2850
- Decision date: 1980-09-09
Classification & Regulation
This clearance is catalogued under FDA product code DRS and 21 CFR 870.2850, within the Cardiovascular review panel as a Class II device.