ClearanceBrief
510(k) K981747 ยท DRS Transducer, Blood-Pressure, Extravascular

BIOTRANS PRESSURE MONITORING KIT MODEL NUMBER BT XXXXXX

ApplicantSunscope Intl., Inc., Newport Beach CA, US
DecisionSubstantially Equivalent, Aug 20, 1998
ReceivedMay 18, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K981747

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.