510(k) K945826 ยท HCC Device, Biofeedback
J & J I-330 SERIES PHYSIOLOGICAL MONITORING & BIOFEEDBACK INSTUMENT AND USE SOFTWARE APPLICATIONS
| Applicant | Medical Device Inspection Co., Inc., Great Neck NY, US |
| Decision | Substantially Equivalent, Aug 4, 1995 |
| Received | Nov 29, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K945826
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.