ClearanceBrief
510(k) K090369 ยท EFB Handpiece, Air-Powered, Dental

PRODRIVE LINE OF DENTAL HANDPIECES

ApplicantProdrive Systems, Inc., Ogdensburg NY, US
DecisionSubstantially Equivalent, Feb 27, 2009
ReceivedFeb 13, 2009
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K090369

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.