Medical Device Manufacturer · US , Salt Lake City , UT

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

5 submissions · 5 cleared · Since 2001

Recent clearances: Curlin 8000 Ambulatory Infusion System, Curlin 8000 Ambulatory Infusion System

5
Total
5
Cleared
0
Denied

Zevex, Inc. has 5 FDA 510(k) cleared medical devices. Based in Salt Lake City, US.

Latest FDA clearance: Oct 2024. Active since 2001. Primary specialty: General Hospital.

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

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

5 devices
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