ClearanceBrief
510(k) K951579 ยท FDF Colonoscope And Accessories, Flexible/Rigid

EC-3800TL, VIDEO COLONOSCOPE

ApplicantPentax Precision Instrument Corp., Miramar FL, US
DecisionSubstantially Equivalent, Mar 21, 1996
ReceivedApr 4, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K951579

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.