ClearanceBrief
510(k) K833265 ยท JAX Pneumotachometer

RESPIRATORY FLOW MODULE

ApplicantThoratec Laboratories Corp., Mchenry IL, US
DecisionSubstantially Equivalent, Nov 28, 1983
ReceivedSep 21, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K833265

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.