510(k) K881852 ยท JJN Apparatus, Electrophoresis, For Clinical Use
REP SP ELECTROPHORESIS SYSTEM CAT NO. 3170
| Applicant | Helena Laboratories, Beaumont TX, US |
| Decision | Substantially Equivalent, Jul 8, 1988 |
| Received | May 2, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K881852
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.