Medical Device Manufacturer · US , Great Bend , KS

Primus Sterilizer Company, LLC - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2009
4
Total
4
Cleared
0
Denied

Primus Sterilizer Company, LLC has 4 FDA 510(k) cleared medical devices. Based in Great Bend, US.

Last cleared in 2023. Active since 2009. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Primus Sterilizer Company, LLC Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Primus Sterilizer Company, LLC

4 devices
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All4 General Hospital 4