510(k) K802396 ยท JJN Apparatus, Electrophoresis, For Clinical Use
GENERAL PROCEDURE AGAROSE FILM
| Applicant | Electrophoresis Corp. of America, Mchenry IL, US |
| Decision | Substantially Equivalent, Nov 26, 1980 |
| Received | Oct 2, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K802396
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.