Medical Device Manufacturer · US , Burlington , MA

Permobil AB - FDA 510(k) Cleared Devices

15 submissions · 14 cleared · Since 1990

Recent clearances: Explorer Mini, F5 Corpus VS

15
Total
14
Cleared
0
Denied

Permobil AB has 14 FDA 510(k) cleared physical medicine devices. Based in Burlington, US.

Historical record: 14 cleared submissions from 1990 to 2020.

Browse the complete list of FDA 510(k) cleared physical medicine devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Permobil AB

15 devices
1-15 of 15
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