ClearanceBrief
510(k) K914557 ยท LKY Device, External Penile Rigidity

ECONOAID

ApplicantGromedco, New Braunfels TX, US
DecisionSubstantially Equivalent, Jan 23, 1992
ReceivedOct 15, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K914557

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.