Medical Device Manufacturer · US , Peoria , IL

Pointcore, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2022
1
Total
1
Cleared
0
Denied

Pointcore, Inc. has 1 FDA 510(k) cleared medical devices. Based in Peoria, US.

Last cleared in 2022. Active since 2022. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Pointcore, Inc. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Mcra, LLC as regulatory consultant.

FDA 510(k) Regulatory Record - Pointcore, Inc.
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