Medical Device Manufacturer · US , Allentown , PA

Serono Baker Diagnostics System - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1991
1
Total
1
Cleared
0
Denied

Serono Baker Diagnostics System has 1 FDA 510(k) cleared medical devices. Based in Allentown, US.

Historical record: 1 cleared submissions from 1991 to 1991. Primary specialty: Hematology.

Browse the FDA 510(k) cleared devices submitted by Serono Baker Diagnostics System Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Serono Baker Diagnostics System

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