Medical Device Manufacturer · US , Soquel , CA

Moe - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1989

6

Total

6

Cleared

0

Denied

FDA 510(k) Regulatory Record - Moe Neurology ✕

6 devices

1-6 of 6

Cleared Mar 23, 1989

BIOFEEDBACK DEVICE ACCESS. PI1,2,3,4,5/LIGHT BAR

Neurology · 125d

Cleared Feb 03, 1989

BIOFEEDBACK DEVICE TG3, TG4

Neurology · 77d

Cleared Feb 02, 1989

BASIC BIOFEEDBACK,TMG4.1, SA1/2, EEG4/5, IR RECEIV

Neurology · 76d

Cleared Feb 02, 1989

BIOFEEDBACK TMG1, 4, BIO1, PA1, 2, BA1/BA30

Neurology · 76d

Cleared Feb 02, 1989

BIOFEEDBACK DEVICE EMG1, EMG ULTRA LOW NOISE OPTI.

Neurology · 76d

Cleared Feb 02, 1989

BIOFEEDBACK EEG1/2, EEG ULTRA LOW NOISE, SYC1

Neurology · 76d