The following data is part of a premarket notification filed by C.r. Bard, Inc. with the FDA for Hickman Titanium Subcutaneous Port.
| Device ID | K870260 |
| 510k Number | K870260 |
| Device Name: | HICKMAN TITANIUM SUBCUTANEOUS PORT |
| Classification | Port & Catheter, Implanted, Subcutaneous, Intravascular |
| Applicant | C.R. BARD, INC. 111 SPRING ST. Murray Hill, NJ 07974 |
| Contact | Catherine V Beath |
| Correspondent | Catherine V Beath C.R. BARD, INC. 111 SPRING ST. Murray Hill, NJ 07974 |
| Product Code | LJT |
| CFR Regulation Number | 880.5965 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-01-23 |
| Decision Date | 1987-04-15 |