ClearanceBrief
510(k) K965101 ยท DXH Transmitters And Receivers, Electrocardiograph, Telephone

CARDIOBEEPER CB-12L

ApplicantMeridian Medical Technologies, Inc., North Attleboro MA, US
DecisionSubstantially Equivalent, Mar 17, 1997
ReceivedDec 20, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K965101

DateFirm and productCodeLinked 510(k)
Feb 20, 2014Zimmer, Inc.
M/DN HUMERAL I/M NAIL. Sizes from 6 MM to 13 MM. Codes starting with 0022541, 002542 and 0022543.
Terminated
HSBNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.