510(k) K884750 ยท GTZ Antisera, All Groups, Streptococcus Spp.
GROUP A STREP, BETA-STREP
| Applicant | Ampcor, Inc., Bridgeport NJ, US |
| Decision | Substantially Equivalent, Dec 22, 1988 |
| Received | Nov 14, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K884750
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.