510(k) K871620 ยท GTZ Antisera, All Groups, Streptococcus Spp.
ALLELIX GROUP A STREPTOCOCCUS DETECTION KIT
| Applicant | Allelix, Inc., Canada L4v 1p1, CA |
| Decision | Substantially Equivalent, Jun 17, 1987 |
| Received | Apr 27, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K871620
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.