ClearanceBrief
510(k) K980480 ยท HQC Unit, Phacofragmentation

SYNTEC VITMAN

ApplicantSyntec, Inc., Chesterfield MO, US
DecisionSubstantially Equivalent, May 4, 1998
ReceivedFeb 3, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K980480

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.