ClearanceBrief
510(k) K884004 ยท GRE Antiserum, Fluorescent, Rubeola

RUBEOLA TEST

ApplicantGull Laboratories, Inc., Salt Lake City UT, US
DecisionSubstantially Equivalent, Dec 5, 1988
ReceivedSep 21, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K884004

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.