ClearanceBrief
510(k) K001306 ยท DQD Stethoscope, Electronic

STETHOS, MODEL STXXYYZZ OR 001 XXX, STETHOS LINK, MODEL SLXXYYZZ OR 002 XXX

ApplicantAndromed, Inc., St.Laurent, Quebec, CA
DecisionSubstantially Equivalent, Jul 20, 2000
ReceivedApr 25, 2000
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K001306

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.