ClearanceBrief
510(k) K854898 ยท KDC Instrument, Surgical, Disposable

ATLANTIC GRASPER

ApplicantEuro-Med Intl., Danville CA, US
DecisionSubstantially Equivalent, May 2, 1986
ReceivedDec 6, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K854898

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.