Medical Device Manufacturer · US , Austin , TX

Mosie Baby - FDA 510(k) Cleared Devices

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

Mosie Baby has 1 FDA 510(k) cleared medical devices. Based in Austin, US.

Last cleared in 2023. Active since 2023. Primary specialty: Obstetrics & Gynecology.

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

510(k) submissions have been managed by Parexel International as regulatory consultant.

FDA 510(k) Regulatory Record - Mosie Baby
1 devices
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