510(k) K800222 ยท DXW System, Phonocatheter, Intracavitary
MODEL 412 ELECTROFLUIDIC MANOMETER
| Applicant | Med-Tek Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Feb 29, 1980 |
| Received | Feb 4, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K800222
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.