ClearanceBrief
510(k) K041395 ยท ITX Transducer, Ultrasonic, Diagnostic

EG-3630UR

ApplicantPentax Precision Instrument Corp., Orangeburg NY, US
DecisionSubstantially Equivalent, Jun 9, 2004
ReceivedMay 26, 2004
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K041395

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.