Medical Device Manufacturer · US , Pleasanton , CA

Phoenix Technology Group, Inc. Dba Phoenix Clinical - FDA 510(k) Clea...

1 submissions · 1 cleared · Since 2017
1
Total
1
Cleared
0
Denied

Phoenix Technology Group, Inc. Dba Phoenix Clinical has 1 FDA 510(k) cleared medical devices. Based in Pleasanton, US.

Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by Phoenix Technology Group, Inc. Dba Phoenix Clinical Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Phoenix Technology Group, Inc. Dba Phoenix Clinical

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