Medical Device Manufacturer · US , New York , NY

Bayer Healthcare, Diagnostics Division - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2004
2
Total
2
Cleared
0
Denied

Bayer Healthcare, Diagnostics Division has 2 FDA 510(k) cleared medical devices. Based in New York, US.

Historical record: 2 cleared submissions from 2004 to 2004. Primary specialty: Chemistry.

Browse the FDA 510(k) cleared devices submitted by Bayer Healthcare, Diagnostics Division Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Bayer Healthcare, Diagnostics Division

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