Medical Device Manufacturer · US , Los Angeles , CA

Automatic Medical Technologies, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2001
2
Total
2
Cleared
0
Denied

Automatic Medical Technologies, Inc. has 2 FDA 510(k) cleared medical devices. Based in Los Angeles, US.

Historical record: 2 cleared submissions from 2001 to 2003. Primary specialty: General Hospital.

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

FDA 510(k) Regulatory Record - Automatic Medical Technologies, Inc.

2 devices
1-2 of 2
Cleared Jan 17, 2003
MAXONE IV FLUID/BLOOD WARMER, MODEL 102
K023653 · LGZ
General Hospital · 79d
Cleared Jun 28, 2001
MAXONE, BLOOD, BLOOD PRODUCTS AND IV FLUID WARMER
K002409 · LGZ
General Hospital · 325d
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