Navilyst Medical, Inc. is one of 4735 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Navilyst Medical, Inc. - FDA 510(k) Cleared Devices
35
Total
33
Cleared
0
Denied
Navilyst Medical, Inc. has 33 FDA 510(k) cleared medical devices. Based in Marlborough, US.
Historical record: 33 cleared submissions from 2009 to 2017. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Navilyst Medical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Navilyst Medical, Inc.
35 devices
Cleared
Feb 03, 2017
PICC Maximal Barrier Nursing Kit
General Hospital
56d
Cleared
Sep 08, 2016
BioFlo Midline Catheter
General Hospital
63d
Cleared
Jun 06, 2016
NMI DUAL PORT II
General Hospital
392d
Cleared
Dec 04, 2015
NMI Port, NMI Port II
General Hospital
28d
Cleared
Sep 24, 2015
Exodus Array Multipurpose Drainage Catheter, Exodus Nuance Nephrostomy...
Gastroenterology & Urology
59d
Cleared
Sep 24, 2015
Xcela PICC with PASV, Xcela Hybrid PICC with PASV, Xcela Power Injectable PICC
General Hospital
29d
Cleared
May 15, 2015
BioFlo Midline Catheter
General Hospital
86d
Cleared
Mar 31, 2015
Xcela Power Injectable PICC
General Hospital
29d
Cleared
Mar 19, 2015
NMI PICC III and NMI PICC IV
General Hospital
27d
Cleared
Oct 14, 2014
PICC Maximal Barrier Nursing Kit
General Hospital
28d
Cleared
Apr 14, 2014
NAMIC RCS SYRINGE
General Hospital
77d
Cleared
Mar 05, 2014
NMI PICC IV
General Hospital
30d