Medical Device Manufacturer · US , Boston , MA

Expandover C/O Hale and Dorr - FDA 510(k) Cleared Devices

1 submissions · 0 cleared · Since 1988
1
Total
0
Cleared
0
Denied

Expandover C/O Hale and Dorr has 0 FDA 510(k) cleared medical devices. Based in Boston, US.

Historical record: 0 cleared submissions from 1988 to 1988. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Expandover C/O Hale and Dorr Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Expandover C/O Hale and Dorr

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