Chemo-Port
510(k) K874184
Chemo-Port is a Class II device made by Hdc Corp., cleared under FDA 510(k) K874184 on 30 Dec 1987, active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK874184 | Date30 Dec 1987 | StatusActive |
Official records
- FDA 510(k) database K874184
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- LJT
- Device class
- Class II
- Regulation
- 21 CFR Part 880.5965
- Advisory committee
- General Hospital
- FDA decision
- SESE Substantially Equivalent
Similar devices
Other devices filed under FDA product code LJT (Port & Catheter, Implanted, Subcutaneous, Intravascular).
- VAXCEL PORT, MODELS 45-336 AND 45-338 by Boston Scientific
- VORTEX ACCESS SYSTEM by Horizon Medical Products, Inc.
- SINGLE LUMEN S.E.A.-PORT VASCULAR ACCESS SYSTEM by Harbor Medical Devices, Inc.
- SEA - PORT INFUSION SET by Harbor Medical Devices, Inc.
- 5F DIGNITY CT TITANIUM PORT by Medical Components, Inc.
- PORT-A-CATH DUAL LUMEN IMPLANTABLE VENOUS by Sims Deltec, Inc.
- THERAPORT LOW-PROFILE VASCULAR ACCESS SYSTEM MODELS 1011 AND 1012 by Biocontrol Technology, Inc.
- X-PROT DUO PORT by C. R. Bard, Inc.
- A PORT IMPLANT VASCULAR ACCESS SYSTEM - DETACHED by Therex Corp.
- VITAL-PORT DUAL LUMEN VASCULAR ACCESS SYSTEM 1121 by Med Institute, Inc.