The following data is part of a premarket notification filed by Navilyst Medical, Inc. with the FDA for Nmi Dual Port Ii.
| Device ID | K151239 |
| 510k Number | K151239 |
| Device Name: | NMI DUAL PORT II |
| Classification | Port & Catheter, Implanted, Subcutaneous, Intravascular |
| Applicant | NAVILYST MEDICAL, INC. 26 FOREST STREET Marlborough, MA 01752 |
| Contact | Robin Fuller |
| Correspondent | Robin Fuller NAVILYST MEDICAL, INC. 26 FOREST STREET Marlborough, MA 01752 |
| Product Code | LJT |
| CFR Regulation Number | 880.5965 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2015-05-11 |
| Decision Date | 2016-06-06 |