ClearanceBrief
510(k) K854561 ยท GES Blade, Scalpel

BLADE, SCALPEL

ApplicantMedelec Intl. Corp., Miami Beach FL, US
DecisionSubstantially Equivalent, Dec 2, 1985
ReceivedNov 14, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K854561

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.