510(k) K895775 ยท KTB Device, Iontophoresis, Specific Uses
CF INDICATOR MODEL 9800 SWEAT TEST SYSTEM
| Applicant | Medtronic Vascular, Minneapolis MN, US |
| Decision | Substantially Equivalent, Apr 23, 1990 |
| Received | Sep 27, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K895775
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.