Maquet GmbH (A Getinge Group Company) - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Maquet GmbH (A Getinge Group Company) has 1 FDA 510(k) cleared medical devices. Based in Rastatt De-Bw, DE.
Latest FDA clearance: Jan 2026. Active since 2026. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Maquet GmbH (A Getinge Group Company) Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Getinge as regulatory consultant.
1 devices