ClearanceBrief
510(k) K962460 ยท FDS Gastroscope And Accessories, Flexible/Rigid

EG-3800T, VIDEO GASTROSCOPE

ApplicantPentax Precision Instrument Corp., Miramar FL, US
DecisionSubstantially Equivalent, Sep 16, 1996
ReceivedJun 25, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K962460

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

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