Medical Device Manufacturer · FR , Paris

Msi France - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2018
1
Total
1
Cleared
0
Denied

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

Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: Dental.

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

FDA 510(k) Regulatory Record - Msi France

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