Moe
Moe holds FDA 510(k) medical device clearances, cleared in 1989.
Top product codes for Moe
Recent clearances by Moe
- K884849 — BIOFEEDBACK DEVICE ACCESS. PI1,2,3,4,5/LIGHT BAR
- K884851 — BIOFEEDBACK DEVICE TG3, TG4
- K884848 — BASIC BIOFEEDBACK,TMG4.1, SA1/2, EEG4/5, IR RECEIV
- K884850 — BIOFEEDBACK TMG1, 4, BIO1, PA1, 2, BA1/BA30
- K884852 — BIOFEEDBACK DEVICE EMG1, EMG ULTRA LOW NOISE OPTI.
- K884853 — BIOFEEDBACK EEG1/2, EEG ULTRA LOW NOISE, SYC1
Data sourced from openFDA. This site is unofficial and independent of the FDA.