510(k) K971708 ยท HCC Device, Biofeedback
PHYSIOLOGICAL MONITORING & BIOFEEDBACK TRAINING DEVICE
| Applicant | J & J Engineering, Inc., Great Neck, NY, US |
| Decision | Substantially Equivalent, Feb 18, 1998 |
| Received | May 8, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K971708
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.