ClearanceBrief
510(k) K050159 ยท DQD Stethoscope, Electronic

MODIFICATION TO: 3M LITTMANN ELECTRONIC STETHOSCOPE, MODEL 3000

Applicant3M Company, St. Paul MN, US
DecisionSubstantially Equivalent, Feb 22, 2005
ReceivedJan 25, 2005
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K050159

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.