ClearanceBrief
510(k) K915808 ยท KYG Device, Irrigation, Ocular Surgery

AQUEOUS PARACENTESIS PIPET

ApplicantVisitec Co., Sarasota FL, US
DecisionSubstantially Equivalent, Mar 19, 1992
ReceivedDec 24, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K915808

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.