This item has been cleaned and treated according to the manufacturer's instructions.
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. div >
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