Medical Device Manufacturer · US , Indianapolis , IN

Nico Corporation - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 2012

Recent clearances: Myriad SPECTRA Light Source, NICO Myriad NOVUS, NICO Myriad

9
Total
9
Cleared
0
Denied

Nico Corporation has 9 FDA 510(k) cleared medical devices. Based in Indianapolis, US.

Latest FDA clearance: Mar 2024. Active since 2012. Primary specialty: Neurology.

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

Regulatory submissions have been managed by Underwriters Laboratories, Inc. and Regulatory Technology Services, LLC.

FDA 510(k) Regulatory Record - Nico Corporation

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