Medical Device Manufacturer · US , Temecula , CA

Merck Millipore , Ltd. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2014

Total

Cleared

Denied

Merck Millipore , Ltd. has 2 FDA 510(k) cleared medical devices. Based in Temecula, US.

Historical record: 2 cleared submissions from 2014 to 2015. Primary specialty: Anesthesiology.

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

FDA 510(k) Regulatory Record - Merck Millipore , Ltd.

2 devices

1-2 of 2