ClearanceBrief
510(k) K914106 ยท FGB Ureteroscope And Accessories, Flexible/Rigid

PENTAX URETERORENOFIBERSCOPE, MODEL FUR-10P

ApplicantPentax Precision Instrument Corp., Orangeburg NY, US
DecisionSubstantially Equivalent, Jan 10, 1992
ReceivedSep 13, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K914106

DateFirm and productCodeLinked 510(k)
Jun 28, 2016Pentax Medical Company
Ureteroscope Intended to provide optical visualization of and therapeutic access to the Urinary Track. This anatomy includes but is not restricted to the organs, tissues and subsystems: Urethra, Bladd
Terminated
FGBNone listed

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