ClearanceBrief
510(k) K040840 ยท ITX Transducer, Ultrasonic, Diagnostic

TERATECH MODEL 10V5 SMART PROBE

ApplicantTeratech Corp., Bainbridge Island WA, US
DecisionSubstantially Equivalent, Apr 14, 2004
ReceivedApr 1, 2004
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K040840

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.