ClearanceBrief
510(k) K894362 ยท KXO Monitor, Pressure, Intrauterine

MODEL DT-IUPC2 TRANSDUCER TIPPED DUAL LUMEN IUP

ApplicantSpectramed, Inc., Oxnard CA, US
DecisionSubstantially Equivalent, Aug 15, 1989
ReceivedJul 14, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K894362

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.