Medical Device Manufacturer · US , St. Louis , MO

Kedly, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2000
2
Total
2
Cleared
0
Denied

FDA 510(k) Regulatory Record - Kedly, Inc. Ear, Nose, Throat ✕

2 devices
1-2 of 2
Cleared Jun 02, 2000
AUDIOSCREENER OAE + ABR
K001058 · EWO
Ear, Nose, Throat · 60d
Cleared Feb 11, 2000
AUDIOSCREENER OAE
K000184 · EWO
Ear, Nose, Throat · 22d
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