ClearanceBrief
510(k) K823434 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording

MIKRO-TIP CATHETER PRESSURE TRANSDUCER

ApplicantMillar Instruments, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Nov 30, 1982
ReceivedNov 16, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K823434

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.