Medical Device Manufacturer · US , Los Angeles , CA

Hill, Farrer & Borrill - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1980
1
Total
1
Cleared
0
Denied

Hill, Farrer & Borrill has 1 FDA 510(k) cleared medical devices. Based in Los Angeles, US.

Historical record: 1 cleared submissions from 1980 to 1980. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Hill, Farrer & Borrill Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Hill, Farrer & Borrill

1 devices
1-1 of 1
Filters