510(k) K842239 ยท GWC Antisera, All Types, Streptococcus Pneumoniae
VENTRESCREEN STREP A TEST
| Applicant | Ventrex Laboratories, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Jul 2, 1984 |
| Received | Jun 5, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K842239
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.