Medical Device Manufacturer · US , Jeffrey , NH

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

26 submissions · 24 cleared · Since 1993
26
Total
24
Cleared
0
Denied

Rusch, Inc. has 24 FDA 510(k) cleared medical devices. Based in Jeffrey, US.

Historical record: 24 cleared submissions from 1993 to 2001. Primary specialty: Anesthesiology.

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

FDA 510(k) cleared devices by Rusch, Inc.

26 devices
1-12 of 26
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