ClearanceBrief
510(k) K921194 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)

HEWLETT-PACKARD CARDIAC CATHETERIZATION RECORDING

ApplicantHewlett-Packard Co., Waltham MA, US
DecisionSubstantially Equivalent, Nov 9, 1992
ReceivedMar 12, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K921194

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.