Medical Device Manufacturer · US , Teaneck , NJ

Duncan Hynd Associates, Ltd. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1998
2
Total
2
Cleared
0
Denied

Duncan Hynd Associates, Ltd. has 2 FDA 510(k) cleared medical devices. Based in Teaneck, US.

Historical record: 2 cleared submissions from 1998 to 2000. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Duncan Hynd Associates, Ltd. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Duncan Hynd Associates, Ltd.
2 devices
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