ClearanceBrief
510(k) K981990 ยท EFB Handpiece, Air-Powered, Dental

MRS-400, MAXI 400, MRSL-400, MAXI 400L

ApplicantD.B.I. America Corp., Tampa FL, US
DecisionSubstantially Equivalent, Jun 22, 1998
ReceivedJun 8, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K981990

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.