Medical Device Manufacturer · US , N. Bay Village , FL

Laura Cattabriga - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2014
2
Total
2
Cleared
0
Denied

Laura Cattabriga has 2 FDA 510(k) cleared medical devices. Based in N. Bay Village, US.

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

Browse the FDA 510(k) cleared devices submitted by Laura Cattabriga Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Laura Cattabriga
2 devices
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