Medical Device Manufacturer · US , Littleton , CO

Regulatory Insight, Inc. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2002

Recent clearances: KEGEL SMART, KEGELSMART PEARL, ETHEREA, EN 600-658, EN 600-666, EN 600-664, EN 600-690, EN 600-651, EN 600-663, EN 600-665 AND EN 600-670 MECHANICAL WHEELCHAIRS

4
Total
4
Cleared
0
Denied

FDA 510(k) Regulatory Record - Regulatory Insight, Inc. General & Plastic Surgery ✕

1 devices
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