ClearanceBrief
510(k) K890876 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)

BP-8800 BLOOD PRESSURE MONITOR

ApplicantColin Medical Instruments Corp., South Plainfield NJ, US
DecisionSubstantially Equivalent, Jun 22, 1989
ReceivedFeb 21, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K890876

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.