ClearanceBrief
510(k) K965012 ยท LPL Lenses, Soft Contact, Daily Wear

LIFESTYLE BREAK THRU (POLYMACON)

ApplicantThe Lifestyle Co., Inc., Morganville NJ, US
DecisionSubstantially Equivalent, Mar 11, 1997
ReceivedDec 16, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K965012

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.