ClearanceBrief
510(k) K880752 ยท GNB Antisera, All Types, Shigella Spp.

PHADEBACT SHIGELLA TEST

ApplicantPharmacia, Inc., Piscataway NJ, US
DecisionSubstantially Equivalent, Feb 17, 1989
ReceivedFeb 24, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K880752

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.