ClearanceBrief
510(k) K130753 ยท LRX Case, Contact Lens

STANDARD CONTACT LENS CASE; FLIP N SLIDE CONTACT LENS CASE

ApplicantWatchdog Group, LC, Clayton MO, US
DecisionSubstantially Equivalent, Jun 13, 2013
ReceivedMar 19, 2013
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K130753

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.