510(k) K930578 ยท HCC Device, Biofeedback
AT33 EMG
| Applicant | Autoject Systems, Inc., Oak Dale IL, US |
| Decision | Substantially Equivalent, May 19, 1995 |
| Received | Feb 4, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K930578
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.