Advanced Respiratory is one of 25373 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Advanced Respiratory - FDA 510(k) Cleared Devices
Recent clearances: THE VEST AIRWAY CLEARANCE SYSTEM, MODEL 104, ABI VEST AIRWAY CLEARANCE SYSTEM
2
Total
2
Cleared
0
Denied
Advanced Respiratory has 2 FDA 510(k) cleared medical devices. Based in St. Paul, US.
Historical record: 2 cleared submissions from 2001 to 2003. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Advanced Respiratory Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Entela, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Advanced Respiratory
2 devices