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. You pay us what you see on the invoice, i. Please make sure it is correct. Or replace item for you free of charge.