Medical Device Manufacturer · US , Soquel , CA

Moe - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1989

6

Total

6

Cleared

0

Denied

Moe has 6 FDA 510(k) cleared medical devices. Based in Soquel, US.

Historical record: 6 cleared submissions from 1989 to 1989. Primary specialty: Neurology.

Browse the FDA 510(k) cleared devices submitted by Moe Filter by specialty or product code using the sidebar.

Moe is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Moe

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