# Moe

- Location (FDA's records): Soquel, CA
- FDA decisions: 6 (1989–1989): 6 510(k) clearances
- Product codes: HCC (6)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K884849: Biofeedback Device Access. PI1,2,3,4,5/Light Bar (Mar 23, 1989)
- K884851: Biofeedback Device TG3, TG4 (Feb 3, 1989)
- K884850: Biofeedback TMG1, 4, BIO1, PA1, 2, BA1/BA30 (Feb 2, 1989)
- K884853: Biofeedback EEG1/2, Eeg Ultra Low Noise, SYC1 (Feb 2, 1989)
- K884848: Basic Biofeedback,TMG4.1, SA1/2, EEG4/5, IR Receiv (Feb 2, 1989)
- K884852: Biofeedback Device EMG1, Emg Ultra Low Noise Opti. (Feb 2, 1989)

Source page: https://510kreport.com/company/moe