ClearanceBrief
510(k) K901748 ยท LRX Case, Contact Lens

KESTREL LENS CASE (208-12NT POLYSTYRENE)

ApplicantKestrel, Columbus IN, US
DecisionSubstantially Equivalent, May 31, 1990
ReceivedApr 17, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K901748

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.