ClearanceBrief
510(k) K875327 ยท DRE Dilator, Vessel, For Percutaneous Catheterization

MODIFIED SELDINGER INITIAL PUNCTURE INSTRUMENT

ApplicantSchneider-Shilley (Usa), Minneapolis MN, US
DecisionSubstantially Equivalent, Mar 25, 1988
ReceivedDec 29, 1987
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K875327

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.