Medical Device Manufacturer · US , Littleton , CO

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

12 submissions · 12 cleared · Since 2002
12
Total
12
Cleared
0
Denied

Dolphin Medical, Inc. has 12 FDA 510(k) cleared anesthesiology devices. Based in Littleton, US.

Historical record: 12 cleared submissions from 2002 to 2006.

Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Dolphin Medical, Inc.
12 devices
1-12 of 12
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