ClearanceBrief
510(k) K940019 ยท FCS Light, Catheter, Fiberoptic, Glass, Ureteral

GABRIEL URETERAL ILLUMINATOR SYSTEM

ApplicantGabriel Medical, Inc., North Attleboro MA, US
DecisionSubstantially Equivalent, May 2, 1994
ReceivedJan 3, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K940019

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.