ClearanceBrief
510(k) K802179 ยท DRS Transducer, Blood-Pressure, Extravascular

CARDIOSCOPE J200

ApplicantTelectronics, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Nov 12, 1980
ReceivedSep 9, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K802179

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.