ClearanceBrief
510(k) K013232 ยท LRX Case, Contact Lens

CYBERCASES BY BAUSCH & LOMB

ApplicantBausch & Lomb, Inc., Rochester NY, US
DecisionSubstantially Equivalent, Nov 20, 2001
ReceivedSep 27, 2001
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K013232

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.