Mano and Mano Proprietary Limited is one of 158 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
Recent clearances: Mano and Mano Personal Lubricant
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.
510(k) submissions have been managed by Clinreg Consulting Services, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Mano and Mano Proprietary Limited
1 devices