Aerocrine AB - FDA 510(k) Cleared Devices
6
Total
5
Cleared
1
Denied
Aerocrine AB has 5 FDA 510(k) cleared medical devices. Based in San Diego, US.
Historical record: 5 cleared submissions from 2003 to 2015. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Aerocrine AB Filter by specialty or product code using the sidebar.
6 devices
Cleared
Feb 26, 2015
NIOX VERO Airway Inflammation Monitor
Chemistry
24d
Cleared
Nov 06, 2014
NIOX VERO AIRWAY INFLAMMATION MONITOR
Chemistry
321d
Cleared
Dec 27, 2012
NIOX PANEL FOR USE WITH THE NIOX MINO AIRWAY INFLAMMATION MONITOR
Chemistry
27d
Cleared
Sep 02, 2010
NIOX MINO MODEL 09-1000
Chemistry
141d
Cleared
Mar 03, 2008
NIOX MINO
Chemistry
153d
Not Cleared
Apr 30, 2003
NIOX ARTICLE NO: 02-1000
Toxicology
43d