Maquet Critica Care AB is one of 59 FDA 510(k) medical device manufacturers from Sweden in the dataset, ranked by real submission volume.
Maquet Critica Care AB - FDA 510(k) Cleared Devices
Recent clearances: Servo-air 4.0 Ventilator System
1
Total
1
Cleared
0
Denied
Maquet Critica Care AB has 1 FDA 510(k) cleared medical devices. Based in Solna, SE.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Maquet Critica Care AB Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Getinge as regulatory consultant.
FDA 510(k) Regulatory Record - Maquet Critica Care AB
1 devices