510(k) K800179 ยท DXW System, Phonocatheter, Intracavitary
INFRASONDE AUTO/INFLATOR ELEC. VIBRATOR
| Applicant | Sphygmetrics, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Feb 11, 1980 |
| Received | Jan 29, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K800179
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.