The following data is part of a premarket notification filed by Gerard Medical Enterprises, Inc. with the FDA for Trimport.
| Device ID | K942623 |
| 510k Number | K942623 |
| Device Name: | TRIMPORT |
| Classification | Port & Catheter, Implanted, Subcutaneous, Intravascular |
| Applicant | GERARD MEDICAL ENTERPRISES, INC. 90 WORCESTER RD. UNIT 2, BOX 6 Charlton, MA 01507 |
| Contact | Richard Cayer Jr. |
| Correspondent | Richard Cayer Jr. GERARD MEDICAL ENTERPRISES, INC. 90 WORCESTER RD. UNIT 2, BOX 6 Charlton, MA 01507 |
| Product Code | LJT |
| CFR Regulation Number | 880.5965 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1994-05-27 |
| Decision Date | 1994-08-23 |