ClearanceBrief
510(k) K870413 ยท DRE Dilator, Vessel, For Percutaneous Catheterization

PERCUTANEOUS SHEATH W/WO MEDI. (5,6,7,8,8.5FR)

ApplicantMedical Surgical Concepts, Inc., Lansdale PA, US
DecisionSubstantially Equivalent, Jun 1, 1987
ReceivedFeb 3, 1987
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K870413

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.