ClearanceBrief
510(k) K961570 ยท FDF Colonoscope And Accessories, Flexible/Rigid

KEC-3840L/F, VIDEO COLONOSCOPE (*L OR F IN MODEL NUMBER DENOTES LENGTH)

ApplicantPentax Precision Instrument Corp., Miramar FL, US
DecisionSubstantially Equivalent, Jun 24, 1996
ReceivedApr 23, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K961570

DateFirm and productCodeLinked 510(k)
Jun 28, 2016Pentax Medical Company
Colonoscope Intended to provide optical visualization of and therapeutic access to the Lower Gastrointestinal Tract. This anatomy includes, but is not restricted to, the organs, tissues and subsystems
Terminated
FDFNone listed

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