ClearanceBrief
510(k) K801239 ยท DRS Transducer, Blood-Pressure, Extravascular

STERILE, DISP DOME, INDIVID. PKG.

ApplicantPacific Domes, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Jul 14, 1980
ReceivedMay 27, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K801239

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.