Clearance Summary
PORT-A-CATH IMPLANTABLE DRUG DELIVERY SYSTEM received FDA 510(k) clearance under submission number K880072, sponsored by Pharmacia Deltec, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 1988-03-29.
- Submission: K880072
- Applicant / Sponsor: Pharmacia Deltec, Inc.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.5965
- Decision date: 1988-03-29
Classification & Regulation
This clearance is catalogued under FDA product code LLD and 21 CFR 880.5965, within the General Hospital review panel as a Class II device.