Mosie Baby is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Mosie Baby - FDA 510(k) Cleared Devices
Recent clearances: Mosie Baby Kit
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