ClearanceBrief
510(k) K973336 ยท JAF Monitor, Ultrasonic, Nonfetal

IMEX STETHODOP

ApplicantImex Medical Systems, Inc., Golden CO, US
DecisionSubstantially Equivalent, Feb 5, 1998
ReceivedSep 4, 1997
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K973336

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.