Medical Device Manufacturer · US , New York , NY

Spark Neuro, Inc. - FDA 510(k) Cleared Devices

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

Spark Neuro, Inc. has 1 FDA 510(k) cleared medical devices. Based in New York, US.

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

Browse the FDA 510(k) cleared devices submitted by Spark Neuro, 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 - Spark Neuro, Inc.
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