ClearanceBrief
510(k) K933152 ยท LYA Splint, Intranasal Septal

MEROCEL MEROSPLINT

ApplicantMerocel Corp., Mystic CT, US
DecisionSubstantially Equivalent, Aug 17, 1993
ReceivedJun 29, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K933152

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.