ClearanceBrief
510(k) K821381 ยท KYB Lens, Guide, Intraocular

IOL FORCEPS

ApplicantCilco, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Jun 14, 1982
ReceivedMay 10, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K821381

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.