Medical Device Manufacturer · US , Provo , UT

Nse Products, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2023
1
Total
1
Cleared
0
Denied

Nse Products, Inc. has 1 FDA 510(k) cleared medical devices. Based in Provo, US.

Last cleared in 2023. Active since 2023. Primary specialty: Neurology.

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

510(k) submissions have been managed by Methodize, Inc. as regulatory consultant.

FDA 510(k) Regulatory Record - Nse Products, Inc.
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