Clearance Summary
CORDIS SUCTION RESERVOIR - MODEL NUMBER: 910-500 received FDA 510(k) clearance under submission number K963839, sponsored by Cordis Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1996-12-12.
- Submission: K963839
- Applicant / Sponsor: Cordis Corp.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class I
- Regulation citation: 21 CFR 878.4680
- Decision date: 1996-12-12
Classification & Regulation
This clearance is catalogued under FDA product code GCY and 21 CFR 878.4680, within the General, Plastic Surgery review panel as a Class I device.