ClearanceBrief
510(k) K883999 ยท GTZ Antisera, All Groups, Streptococcus Spp.

QUIDEL GROUP A STREP TEST

ApplicantQuidel Corp., San Diego CA, US
DecisionSubstantially Equivalent, Oct 12, 1988
ReceivedSep 19, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K883999

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.