Medical Device Manufacturer · SE , Sweden

Astra Meditec AB - FDA 510(k) Cleared Devices

3 submissions · 2 cleared · Since 1988
3
Total
2
Cleared
0
Denied

Astra Meditec AB has 2 FDA 510(k) cleared medical devices. Based in Sweden, SE.

Historical record: 2 cleared submissions from 1988 to 1993.

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

FDA 510(k) Regulatory Record - Astra Meditec AB

3 devices
1-3 of 3
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