ClearanceBrief
510(k) K854994 ยท KYB Lens, Guide, Intraocular

BARTELL SMALL INCISION LENS GLIDE

ApplicantMicrotech, Inc., Doylestown PA, US
DecisionSubstantially Equivalent, Feb 4, 1986
ReceivedDec 12, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K854994

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.