Medical Device Manufacturer · DE , Gottingen, Germany

Sartorius, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1985
1
Total
1
Cleared
0
Denied

Sartorius, Inc. has 1 FDA 510(k) cleared medical devices. Based in Gottingen, Germany, DE.

Historical record: 1 cleared submissions from 1985 to 1985. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Sartorius, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Sartorius, Inc.

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