Mano and Mano Proprietary Limited is one of 80 FDA 510(k) medical device manufacturers from Australia in the dataset, ranked by real submission volume.
Mano and Mano Proprietary Limited - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Mano and Mano Proprietary Limited has 1 FDA 510(k) cleared medical devices. Based in Moorabbin, AU.
Historical record: 1 cleared submissions from 2016 to 2016. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Mano and Mano Proprietary Limited Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Mano and Mano Proprietary Limited
1 devices