510(k) K882554 ยท EGJ Device, Iontophoresis, Other Uses
MEDITRODE KIT
| Applicant | Life-Tech Intl., Inc., Houston TX, US |
| Decision | Unknown, Dec 23, 1988 |
| Received | Jun 21, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K882554
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.