ClearanceBrief
510(k) K972033 ยท EIA Unit, Operative Dental

PLANMECA INTRACAM

ApplicantPlanmeca Oy, Helsinki, FI
DecisionSubstantially Equivalent, Jun 20, 1997
ReceivedJun 2, 1997
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K972033

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.