Medical Device Manufacturer · US , Los Angeles , CA

Cewal, Inc. Dba Premiere Enterprises - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2018

Total

Cleared

Denied

Cewal, Inc. Dba Premiere Enterprises has 1 FDA 510(k) cleared medical devices. Based in Los Angeles, US.

Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: Obstetrics & Gynecology.

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

FDA 510(k) cleared devices by Cewal, Inc. Dba Premiere Enterprises

1 devices

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