ClearanceBrief
510(k) K921601 ยท JES Floss, Dental

ULTRADENT PROD RETRACT CORD/ACCESSORY PRODUCT LINE

ApplicantUltradent Products, Inc., Salt Lake City UT, US
DecisionSubstantially Equivalent, Jun 16, 1992
ReceivedApr 3, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K921601

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.