Food and Drug Administration and state and local regulatory agencies. The Fingertip Pulse Oximeter is certified with the US FDA 510K No. K070371, the CE & TUV of Eureope and it is on the Australian Register of Therapeutic Goods(ARTG) with the code 136606. The Powered Surgical Instrument / Speed 808 System is certified with the US FDA 510(k) Number:K132989.
The Powered Surgical Instrument / Hair Remove Device is certified with the US FDA 510(k) Number:K180353. The Powered Surgical Instrument / Hair Remove System is certified with the US FDA 510(k) Number:K141973. Massager, vacuum, light induced heating / Slimming Treatment Device is certified with the US FDA 510(k) Number:K161892. This item is in the category "Business & Industrial\Healthcare, Lab & Dental\Medical & Lab Equipment, Devices\Ultrasound Machines". The seller is "perfectshop999" and is located in this country: CN.This item can be shipped to United States.