Medical Device Manufacturer · US , Foster , RI

Fresenius AG - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1996
2
Total
2
Cleared
0
Denied

Fresenius AG has 2 FDA 510(k) cleared medical devices. Based in Foster, US.

Historical record: 2 cleared submissions from 1996 to 1997. Primary specialty: Anesthesiology.

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

FDA 510(k) Regulatory Record - Fresenius AG
2 devices
1-2 of 2
Cleared Jun 13, 1997
C.A.T.S CONTINUOUS AUTOTRANSFUSION SYSTEM, AT1 AUTOTRANSFUSION SET, PSQ SET
K971274 · CAC
Anesthesiology · 67d
Cleared Jul 31, 1996
C.A.T.S. CONTINUOUS AUTOTRANSFUSION SYSTEM
K960006 · CAC
Anesthesiology · 211d
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