Clearance Summary
ANGIOCATH SIDEHOLDER DRAINAGE CATHETER received FDA 510(k) clearance under submission number K950437, sponsored by Becton Dickinson Vascular Access, Inc.. 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 1995-03-14.
- Submission: K950437
- Applicant / Sponsor: Becton Dickinson Vascular Access, Inc.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class I
- Regulation citation: 21 CFR 878.4200
- Decision date: 1995-03-14
Classification & Regulation
This clearance is catalogued under FDA product code GBX and 21 CFR 878.4200, within the General, Plastic Surgery review panel as a Class I device.