ClearanceBrief
510(k) K820410 ยท LOX Catheters, Transluminal Coronary Angioplasty, Percutaneous

HEMOTEC HEPCON/SYSTEM FOUR & FOUR P

ApplicantHemotec, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Apr 9, 1982
ReceivedFeb 12, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K820410

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.