Clearance Summary
ARTERIAL BUBBLE TRAP K-20 received FDA 510(k) clearance under submission number K803102, sponsored by Delta Medical Industries. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1980-12-22.
- Submission: K803102
- Applicant / Sponsor: Delta Medical Industries
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.4205
- Decision date: 1980-12-22
Classification & Regulation
This clearance is catalogued under FDA product code KRL and 21 CFR 870.4205, within the Cardiovascular review panel as a Class II device.