Medical Device Manufacturer · SE , Stockholm

Coala Life AB - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2019
2
Total
2
Cleared
0
Denied

Coala Life AB has 2 FDA 510(k) cleared medical devices. Based in Stockholm, SE.

Last cleared in 2022. Active since 2019. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Coala Life AB Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Acknowledge Regulatory Strategies as regulatory consultant.

FDA 510(k) Regulatory Record - Coala Life AB

2 devices
1-2 of 2
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All2 Cardiovascular 2