510(k) K964208 ยท EGJ Device, Iontophoresis, Other Uses
MD-1A GALVANIC UNIT
| Applicant | R. A. Fischer Co. Corp., Glendale CA, US |
| Decision | Substantially Equivalent, Apr 30, 1997 |
| Received | Oct 4, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K964208
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.