ClearanceBrief
510(k) K904021 ยท JDC Prosthesis, Elbow, Constrained, Cemented

PNEUMOTHORAX KIT, MODIFICATION

ApplicantArrow Intl., Inc., Reading PA, US
DecisionSubstantially Equivalent, Oct 9, 1990
ReceivedAug 29, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K904021

DateFirm and productCodeLinked 510(k)
Oct 24, 2017Arrow International Inc
Pneumothorax Kit
Terminated
KDDNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.