ClearanceBrief
510(k) K921315 ยท GCT Light Source, Endoscope, Xenon Arc

PENTAX XENON LIGHT SOURCE

ApplicantPentax Precision Instrument Corp., Orangeburg NY, US
DecisionSubstantially Equivalent, Jun 25, 1993
ReceivedMar 18, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K921315

No recall in the FDA data names this 510(k).

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