Medical Device Manufacturer · US , Indianola , PA

Bayer U.S., LLC - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2018

Total

Cleared

Denied

Bayer U.S., LLC has 1 FDA 510(k) cleared medical devices. Based in Indianola, US.

Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Bayer U.S., LLC Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Bayer U.S., LLC

1 devices

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