Mankind Pharma Limited - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Mankind Pharma Limited has 1 FDA 510(k) cleared medical devices. Based in New Delhi, IN.
Latest FDA clearance: Apr 2024. Active since 2024. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Mankind Pharma Limited Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Lifestar Pharma, LLC (A Mankind Group Company) as regulatory consultant.
FDA 510(k) Regulatory Record - Mankind Pharma Limited
1 devices