Medical Device Manufacturer · US , St. Paul , MN

Advanced Respiratory - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2001
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.

FDA 510(k) Regulatory Record - Advanced Respiratory
2 devices
1-2 of 2
Cleared Feb 21, 2003
THE VEST AIRWAY CLEARANCE SYSTEM, MODEL 104
K024309 · BYI
Anesthesiology · 59d
Cleared Oct 09, 2001
ABI VEST AIRWAY CLEARANCE SYSTEM
K012928 · BYI
Anesthesiology · 39d
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