ClearanceBrief
510(k) K930558 ยท DPS Electrocardiograph

MORTARA INSTRUMENT, INC. E-SCRIBE

ApplicantMortara Instrument, Inc., Milwaukee WI, US
DecisionSubstantially Equivalent, Apr 27, 1993
ReceivedFeb 3, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K930558

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.