The following data is part of a premarket notification filed by Navilyst Medical, Inc. with the FDA for Nmi Picc Iii Catheter, Nmi Hpicc Iii Catheter.
Device ID | K131942 |
510k Number | K131942 |
Device Name: | NMI PICC III CATHETER, NMI HPICC III CATHETER |
Classification | Catheter, Intravascular, Therapeutic, Long-term Greater Than 30 Days |
Applicant | NAVILYST MEDICAL, INC. 26 FOREST STREET Marlborough, MA 01752 |
Contact | Lorraine M Hanley |
Correspondent | Lorraine M Hanley NAVILYST MEDICAL, INC. 26 FOREST STREET Marlborough, MA 01752 |
Product Code | LJS |
CFR Regulation Number | 880.5970 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2013-06-27 |
Decision Date | 2013-07-31 |
Summary: | summary |