Medical Device Manufacturer · US , Ft. Lauderdale , FL

Drip Alert, Inc.

1 submissions · 1 cleared · Since 2003
1
Total
1
Cleared
0
Denied

Drip Alert, Inc. has 1 FDA 510(k) cleared medical devices. Based in Ft. Lauderdale, US.

Historical record: 1 cleared submissions from 2003 to 2003. Primary specialty: General Hospital.

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

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