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Moe

6 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
BIOFEEDBACK DEVICE ACCESS. PI1,2,3,4,5/LIGHT BAR (K884849)Moe1989-03-23
BIOFEEDBACK DEVICE TG3, TG4 (K884851)Moe1989-02-03
BIOFEEDBACK TMG1, 4, BIO1, PA1, 2, BA1/BA30 (K884850)Moe1989-02-02
BASIC BIOFEEDBACK,TMG4.1, SA1/2, EEG4/5, IR RECEIV (K884848)Moe1989-02-02
BIOFEEDBACK EEG1/2, EEG ULTRA LOW NOISE, SYC1 (K884853)Moe1989-02-02
BIOFEEDBACK DEVICE EMG1, EMG ULTRA LOW NOISE OPTI. (K884852)Moe1989-02-02

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Every clearance here is in the API, with alerts when new ones post.