510(k) K883960 ยท FFT Electrode, Ph, Stomach
GIPHY MONITOR
| Applicant | Vascular Technology Incorporated, Chelmsford MA, US |
| Decision | Substantially Equivalent, Oct 4, 1989 |
| Received | Sep 20, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K883960
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.