510(k) K895365 ยท EGJ Device, Iontophoresis, Other Uses
MD-2 IONTOPHORESIS UNIT
| Applicant | R. A. Fischer Co. Corp., Glendale CA, US |
| Decision | Unknown, Jun 26, 1990 |
| Received | Aug 28, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K895365
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.