ClearanceBrief
510(k) K930628 ยท KYB Lens, Guide, Intraocular

KLAAS IOL LENSFOLDER

ApplicantBova Intl., Fort Worth TX, US
DecisionSubstantially Equivalent, Feb 7, 1995
ReceivedFeb 8, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K930628

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.