ClearanceBrief
510(k) K000070 ยท KOD Catheter, Urological

FLOCATH

ApplicantRusch Intl., Jeffrey NH, US
DecisionSubstantially Equivalent, Feb 18, 2000
ReceivedJan 10, 2000
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K000070

DateFirm and productCodeLinked 510(k)
Jul 1, 2019Teleflex Medical
Rusch EasyCath Kit
Terminated
KODNone listed
Jun 9, 2014Teleflex Medical
RUSCH Easy Cath Coude Kit, 10 FR, Rx Only, Sterile, Distributed by: Teleflex Medical, Research Triangle Park, NC 27708. A tubular device that is inserted through the urethera and is used to pass flui
Terminated
KODNone listed

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