510(k) K875369 ยท FFT Electrode, Ph, Stomach
MODEL ISO-2001 UNIV. PATIENT ISOLATION CIRCUIT
| Applicant | Diamond Medical, Inc., St. Paul MN, US |
| Decision | Substantially Equivalent, Feb 5, 1988 |
| Received | Dec 31, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K875369
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.