Clearance Summary
FLUSH DEVICE received FDA 510(k) clearance under submission number K833170, sponsored by Transamerica Delaval, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1984-08-12.
- Submission: K833170
- Applicant / Sponsor: Transamerica Delaval, Inc.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2850
- Decision date: 1984-08-12
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.