The following data is part of a premarket notification filed by Pharmacia, Inc. with the FDA for Port-a-cath Implantable Cath. Sys.
| Device ID | K830730 |
| 510k Number | K830730 |
| Device Name: | PORT-A-CATH IMPLANTABLE CATH. SYS |
| Classification | Port & Catheter, Implanted, Subcutaneous, Intravascular |
| Applicant | PHARMACIA, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | LJT |
| CFR Regulation Number | 880.5965 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-03-08 |
| Decision Date | 1983-06-30 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 30610586028469 | K830730 | 000 |
| 10610586023811 | K830730 | 000 |
| 10610586023804 | K830730 | 000 |
| 10610586023798 | K830730 | 000 |
| 10610586023781 | K830730 | 000 |
| 10610586023774 | K830730 | 000 |
| 10610586023767 | K830730 | 000 |
| 10610586023750 | K830730 | 000 |
| 10610586023743 | K830730 | 000 |
| 10610586023736 | K830730 | 000 |
| 10610586023729 | K830730 | 000 |
| 10610586023712 | K830730 | 000 |
| 10610586023545 | K830730 | 000 |
| 10610586023538 | K830730 | 000 |
| 10610586023521 | K830730 | 000 |
| 10610586023514 | K830730 | 000 |
| 10610586023828 | K830730 | 000 |
| 10610586023835 | K830730 | 000 |
| 10610586023842 | K830730 | 000 |
| 30610586028063 | K830730 | 000 |
| 30610586028056 | K830730 | 000 |
| 30610586024126 | K830730 | 000 |
| 30610586024119 | K830730 | 000 |
| 30610586024089 | K830730 | 000 |
| 30610586024072 | K830730 | 000 |
| 30610586024065 | K830730 | 000 |
| 30610586024058 | K830730 | 000 |
| 30610586024041 | K830730 | 000 |
| 30610586024034 | K830730 | 000 |
| 30610586024027 | K830730 | 000 |
| 30610586024010 | K830730 | 000 |
| 30610586024003 | K830730 | 000 |
| 30610586023990 | K830730 | 000 |
| 10610586025150 | K830730 | 000 |
| 10610586023507 | K830730 | 000 |