Medical Device Manufacturer · FR , Paris

H4D Sas - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2017

Recent clearances: Consult Station TS

1
Total
1
Cleared
0
Denied

H4D Sas has 1 FDA 510(k) cleared medical devices. Based in Paris, FR.

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

Browse the FDA 510(k) cleared devices submitted by H4D Sas Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Voisin Consulting Life Sciences as regulatory consultant.

FDA 510(k) Regulatory Record - H4D Sas

1 devices
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