FDA for Handpiece: 510(K) Number: K181691, Regulation Number: 872.4200, Classification Product Code: EFB, Subsequent Product Code: EGS. FDA for Curing Light: 510(K) Number: K192233, Regulation Number: 21 CFR 872.6070, Product Code: EBZ.
(Infection and dental chair interface pollution;. FDA for Handpiece b) Anti-suction design, prevent sand powder and water absorption, prevent cross-. c) Input air pressure: 35 bar ~ 45 bar ( 350 -450 kpa );.
FDA for Handpiece: 510(K) Number: K181691, Regulation Number: 872.4200, Classification Product Code: EFB, Subsequent Product Code: EGS. FDA for Curing Light: 510(K) Number: K192233, Regulation Number: 21 CFR 872.6070, Product Code: EBZ.
FDA for Handpiece: 510(K) Number: K181691, Regulation Number: 872.4200, Classification Product Code: EFB, Subsequent Product Code: EGS. FDA for Curing Light: 510(K) Number: K192233, Regulation Number: 21 CFR 872.6070, Product Code: EBZ.
(A) Supragingival and subgingival prophy, comprehensive plaque removal and. infection and dental chair interface pollution;. b) Anti-suction design, prevent sand powder and water absorption, prevent cross-.
