Medical Device Manufacturer · CA , Louiseville

Entreprise Premont, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2022

Total

Cleared

Denied

Entreprise Premont, Inc. has 1 FDA 510(k) cleared medical devices. Based in Louiseville, CA.

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

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

FDA 510(k) cleared devices by Entreprise Premont, Inc.

1 devices

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