Medical Device Manufacturer · US , New York , NY

Memory MD, Inc. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2018
3
Total
3
Cleared
0
Denied

Memory MD, Inc. has 3 FDA 510(k) cleared medical devices. Based in New York, US.

Last cleared in 2021. Active since 2018. Primary specialty: Neurology.

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

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

FDA 510(k) Regulatory Record - Memory MD, Inc.

3 devices
1-3 of 3
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All3 Neurology 3