ClearanceBrief
510(k) K951808 ยท IYE Accelerator, Linear, Medical

MED-TEC REDI-FOAM

ApplicantMedtec, Inc., Orange City IA, US
DecisionSubstantially Equivalent, Jul 6, 1995
ReceivedApr 19, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K951808

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.