ClearanceBrief
510(k) K992388 ยท DPW Flowmeter, Blood, Cardiovascular

ROSSMAX AUTOMATIC WRISTWATCH BLOOD PRESSURE MONITOR, MODEL RM-4200

ApplicantRossmax International , Ltd., Taipei, TW
DecisionSubstantially Equivalent, Aug 3, 1999
ReceivedJul 19, 1999
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K992388

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.