Medical Device Manufacturer · FR , Neuilly Sur Seine

Hinlab Sas - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2024
1
Total
1
Cleared
0
Denied

Hinlab Sas has 1 FDA 510(k) cleared medical devices. Based in Neuilly Sur Seine, FR.

Latest FDA clearance: Nov 2024. Active since 2024. Primary specialty: Cardiovascular.

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

FDA 510(k) cleared devices by Hinlab Sas

1 devices
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All1 Cardiovascular 1