Aerocrine AB
Aerocrine AB appears in FDA public data with 0 recalls, 6 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Feb 26, 2015.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 6
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K150233 | NIOX VERO Airway Inflammation Monitor | Feb 26, 2015 |
| K133898 | NIOX VERO AIRWAY INFLAMMATION MONITOR | Nov 6, 2014 |
| K123683 | NIOX PANEL FOR USE WITH THE NIOX MINO AIRWAY INFLAMMATION MONITOR | Dec 27, 2012 |
| K101034 | NIOX MINO MODEL 09-1000 | Sep 2, 2010 |
| K072816 | NIOX MINO | Mar 3, 2008 |
| DEN030001 | NIOX ARTICLE NO: 02-1000 | Apr 30, 2003 |