Medical Device Manufacturer · IT , Pomezia Rm

Metaltronica Spa - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2021
1
Total
1
Cleared
0
Denied

Metaltronica Spa has 1 FDA 510(k) cleared medical devices. Based in Pomezia Rm, IT.

Last cleared in 2021. Active since 2021. Primary specialty: Radiology.

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

510(k) submissions have been managed by Emergo Europe Consulting as regulatory consultant.

FDA 510(k) Regulatory Record - Metaltronica Spa
1 devices
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