510(k) K881343 ยท GXY Electrode, Cutaneous
DURADERM BUTTERFLY
| Applicant | Sentry Medical Products, Inc., Santa Ana CA, US |
| Decision | Substantially Equivalent, May 4, 1988 |
| Received | Mar 30, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K881343
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.