ClearanceBrief
510(k) K011222 ยท EIA Unit, Operative Dental

PORTABELL, MODEL 4200

ApplicantBell Dental Products, LLC, Denver CO, US
DecisionSubstantially Equivalent, Jun 25, 2001
ReceivedApr 20, 2001
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K011222

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.