Medical Device Manufacturer · US , Davenport , IA

Carleton Life Support Systems, Inc. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2005
3
Total
3
Cleared
0
Denied

Carleton Life Support Systems, Inc. has 3 FDA 510(k) cleared medical devices. Based in Davenport, US.

Historical record: 3 cleared submissions from 2005 to 2008. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Carleton Life Support Systems, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Carleton Life Support Systems, Inc.
3 devices
1-3 of 3
Cleared Dec 22, 2008
AIRCRAFT MEDICAL OXYGEN GENERATION SYSTEM (AMOGS)
K082829 · OLF
Anesthesiology · 88d
Cleared Oct 25, 2007
DEPLOYABLE OXYGEN GENERATION SYSTEM - MEDIUM (DOGS-M)
K071904 · CAW
Anesthesiology · 107d
Cleared Sep 27, 2005
PATIENT VENTILATION OXYGEN CONCENTRATING SYSTEM, HIGH FLOW (PVOCS HF)
K051887 · CAW
Anesthesiology · 77d
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