ClearanceBrief
510(k) K043278 ยท ITX Transducer, Ultrasonic, Diagnostic

TERATECH MODEL 8IOC4, 8IOL4 & 10LAP4 PROBES

ApplicantTeratech Corp., Bainbridge Island WA, US
DecisionSubstantially Equivalent, Dec 13, 2004
ReceivedNov 26, 2004
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K043278

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.