Company ยท US
Moe
FDA 510(k) clearances and medical device recalls filed under this name, 1989 to 1989. Name variants (Inc, Corp, punctuation) are merged.
6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
| Code | Device | Records |
|---|---|---|
| HCC | Device, Biofeedback | 6 |
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Mar 23, 1989 | K884849 | BIOFEEDBACK DEVICE ACCESS. PI1,2,3,4,5/LIGHT BAR Moe | HCC |
| Feb 3, 1989 | K884851 | BIOFEEDBACK DEVICE TG3, TG4 Moe | HCC |
| Feb 2, 1989 | K884853 | BIOFEEDBACK EEG1/2, EEG ULTRA LOW NOISE, SYC1 Moe | HCC |
| Feb 2, 1989 | K884852 | BIOFEEDBACK DEVICE EMG1, EMG ULTRA LOW NOISE OPTI. Moe | HCC |
| Feb 2, 1989 | K884850 | BIOFEEDBACK TMG1, 4, BIO1, PA1, 2, BA1/BA30 Moe | HCC |
| Feb 2, 1989 | K884848 | BASIC BIOFEEDBACK,TMG4.1, SA1/2, EEG4/5, IR RECEIV Moe | HCC |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||