ClearanceBrief
510(k) K100833 ยท EFB Handpiece, Air-Powered, Dental

SYLE SMARTIP

ApplicantOsspray, Ltd., Gainesville FL, US
DecisionSubstantially Equivalent, Jun 3, 2010
ReceivedMar 24, 2010
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K100833

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.