ClearanceBrief
510(k) K895682 ยท GDX Scalpel, One-Piece

VESSEL LOOPS

ApplicantApplied Medical Technologies, Independence OH, US
DecisionSubstantially Equivalent, Oct 24, 1989
ReceivedSep 21, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K895682

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.