Medical Device Manufacturer · US , Germantown , MD

Automedx, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2007
2
Total
2
Cleared
0
Denied

Automedx, Inc. has 2 FDA 510(k) cleared medical devices. Based in Germantown, US.

Historical record: 2 cleared submissions from 2007 to 2014. Primary specialty: Anesthesiology.

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

FDA 510(k) Regulatory Record - Automedx, Inc.
2 devices
1-2 of 2
Cleared Mar 21, 2014
SAVE II, SAVE II BASIC
K131877 · BTL
Anesthesiology · 269d
Cleared Sep 06, 2007
SAVE-SIMPLIFIED AUTOMATED VENTILATOR, MODELS: 550X10, 600X10 AND 600X12
K071221 · BTL
Anesthesiology · 127d
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