Medical Device Manufacturer · US , Miami , FL

Fridababy, LLC - FDA 510(k) Cleared Devices

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

Fridababy, LLC has 1 FDA 510(k) cleared medical devices. Based in Miami, US.

Last cleared in 2022. Active since 2022. Primary specialty: Neurology.

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

510(k) submissions have been managed by I-Squared Group, LLC as regulatory consultant.

FDA 510(k) Regulatory Record - Fridababy, LLC
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