Clearance Summary
MODIFICATION TO: GP GENERAL PURPOSE DRAINAGE CATHETER, MINI-PIG DRAINAGE CATHETER, NEPHROSTOMY CATHETER, BILIARY received FDA 510(k) clearance under submission number K041995, sponsored by Uresil, LLC. The device was reviewed via the Special premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2004-08-19.
- Submission: K041995
- Applicant / Sponsor: Uresil, LLC
- Clearance pathway: Special
- Review panel: General, Plastic Surgery
- Device class: Class I
- Regulation citation: 21 CFR 878.4200
- Decision date: 2004-08-19
Classification & Regulation
This clearance is catalogued under FDA product code GBO and 21 CFR 878.4200, within the General, Plastic Surgery review panel as a Class I device.