Medical Device Manufacturer · US , Elk Grove Village , IL

Mid-America Safety Corp. - FDA 510(k) Cleared Devices

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

Mid-America Safety Corp. has 1 FDA 510(k) cleared medical devices. Based in Elk Grove Village, US.

Last cleared in 2021. Active since 2021. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Mid-America Safety Corp. Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Mid-America Safety Corp.

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