ClearanceBrief
510(k) K893232 ยท DSK Computer, Blood-Pressure

MODEL V420 DIRECT PRESSURE MONITOR & 427 WAVEFORM

ApplicantCamino Laboratories, Inc., San Diego CA, US
DecisionSubstantially Equivalent, Jul 14, 1989
ReceivedApr 28, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K893232

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.