510(k) K811083 ยท FFT Electrode, Ph, Stomach
ESOPHAGEAL MOTILITY PROBE
| Applicant | Konigsberg Instruments, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Aug 13, 1981 |
| Received | Apr 21, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K811083
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.