ClearanceBrief
510(k) K874680 ยท FCS Light, Catheter, Fiberoptic, Glass, Ureteral

LASEGUIDE 600A, 600B, 400A, AND 400B

ApplicantLaser Peripherals, LLC, Hingham MA, US
DecisionSubstantially Equivalent, Mar 23, 1988
ReceivedNov 13, 1987
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K874680

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.