ClearanceBrief
510(k) K780483 ยท EFB Handpiece, Air-Powered, Dental

FIBER OPTIC HANDPIECE

ApplicantSyntex Corp., Mchenry IL, US
DecisionSubstantially Equivalent, Apr 28, 1978
ReceivedMar 27, 1978
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K780483

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.