ClearanceBrief
510(k) K083903 ยท DQD Stethoscope, Electronic

3M LITTMANN ELECTRONIC STETHOSCOPE, MODEL 3200

Applicant3M Company, St. Paul MN, US
DecisionSubstantially Equivalent, Jul 15, 2009
ReceivedDec 29, 2008
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K083903

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.