ClearanceBrief
510(k) K802332 ยท KYG Device, Irrigation, Ocular Surgery

INTRAJECT

ApplicantGeneral Medical Engineering Corp., Mchenry IL, US
DecisionSubstantially Equivalent, Dec 22, 1980
ReceivedSep 23, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K802332

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.