The following data is part of a premarket notification filed by Medcomp with the FDA for T3.
| Device ID | K123292 |
| 510k Number | K123292 |
| Device Name: | T3 |
| Classification | Catheter, Hemodialysis, Triple Lumen, Non-implanted |
| Applicant | MEDCOMP 1499 DELP DR. Harleysville, PA 19438 |
| Contact | Timothy Holwick |
| Correspondent | Timothy Holwick MEDCOMP 1499 DELP DR. Harleysville, PA 19438 |
| Product Code | NIE |
| CFR Regulation Number | 876.5540 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2012-10-22 |
| Decision Date | 2013-06-11 |
| Summary: | summary |