ClearanceBrief
510(k) K895735 ยท LYY Latex Patient Examination Glove

DESERET MULTILUMEN SUBCLAVIAN CATHETER

ApplicantDeseret Medical, Inc., Sandy UT, US
DecisionSubstantially Equivalent, May 18, 1990
ReceivedSep 27, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K895735

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.