Clearance Summary
OMNICORDER, MODEL 464 received FDA 510(k) clearance under submission number K990027, sponsored by Del Mar Avionics. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1999-02-09.
- Submission: K990027
- Applicant / Sponsor: Del Mar Avionics
- Clearance pathway: Abbreviated
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2800
- Decision date: 1999-02-09
Classification & Regulation
This clearance is catalogued under FDA product code DSH and 21 CFR 870.2800, within the Cardiovascular review panel as a Class II device.