ClearanceBrief
510(k) K896265 ยท GTZ Antisera, All Groups, Streptococcus Spp.

QUIDEL GROUP B STREP TEST

ApplicantQuidel Corp., San Diego CA, US
DecisionSubstantially Equivalent, Feb 16, 1990
ReceivedOct 31, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K896265

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.