Novo Nordisk, Inc. - FDA 510(k) Cleared Devices
14
Total
14
Cleared
0
Denied
FDA 510(k) cleared devices by Novo Nordisk, Inc. General Hospital ✕
14 devices
Cleared
Aug 25, 2023
NovoFine® Plus
General Hospital
116d
Cleared
Jun 23, 2021
NovoFine
General Hospital
142d
Cleared
Dec 19, 2020
NovoFine Plus 32G Tip x 4 mm
General Hospital
151d
Cleared
Dec 17, 2018
NovoPen Echo Dial-A-Dose Insulin Delivery Device (Pen Injector)
General Hospital
104d
Cleared
Jan 17, 2018
NovoFine 32G Tip (0.23/0.25) x 6 mm ETW (extra thin wall)
General Hospital
65d
Cleared
Oct 18, 2016
NovoPen Echo
General Hospital
29d
Cleared
Jul 31, 2015
NovoPen Echo Dial-A-Dose Insulin Delivery Device (Pen Injector)
General Hospital
121d
Cleared
May 21, 2014
NOVOFINE PLUS 32G 4 MM
General Hospital
163d
Cleared
Aug 15, 2013
NOVOPEN ECHO, A DIAL A DOSE INSULIN DELIVERY PEN
General Hospital
251d
Cleared
Jun 18, 2010
NOVOTWIST NEEDLE, MODELS 30G * 8MM (1/3) 32 G TIP * 5 MM(1/5')
General Hospital
260d
Cleared
Feb 01, 2010
FLEXPEN NEEDLE
General Hospital
381d
Cleared
Nov 21, 2006
FLEXPEN NEEDLE
General Hospital
88d