Medical Device Manufacturer · US , Cranberry , PA

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

1 submissions · 1 cleared · Since 2022

Total

Cleared

Denied

Omnicell, Inc. has 1 FDA 510(k) cleared medical devices. Based in Cranberry, US.

Last cleared in 2022. Active since 2022. Primary specialty: General Hospital.

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

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

1 devices

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