510(k) K781629 ยท JKA Tubes, Vials, Systems, Serum Separators, Blood Collection
SERI-SEP SERUM/PLASMA ISLOLATOR
| Applicant | Wako Intl., Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Oct 27, 1978 |
| Received | Sep 25, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K781629
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.