Medical Device Manufacturer · CH , Schutzengraben 20

Jextrag Schaffhausen AG - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1989
1
Total
1
Cleared
0
Denied

Jextrag Schaffhausen AG has 1 FDA 510(k) cleared medical devices. Based in Schutzengraben 20, CH.

Historical record: 1 cleared submissions from 1989 to 1989. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Jextrag Schaffhausen AG Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Jextrag Schaffhausen AG

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