Medical Device Manufacturer · FR , Varilhes

Argene SA - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2013
1
Total
1
Cleared
0
Denied

Argene SA has 1 FDA 510(k) cleared medical devices. Based in Varilhes, FR.

Historical record: 1 cleared submissions from 2013 to 2013. Primary specialty: Microbiology.

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

Argene SA — FDA 510(k) Products and Clearance History

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All1 Microbiology 1