FDA
declaration :
Statement：The sale of this item
may be subject to regulation by the U.S. Food and Drug Administration and state
and local regulatory agencies. If so, do not bid on this item unless you are an
authorized purchaser. If the item is subject to FDA regulation, I will verify
your status as an authorized purchaser of this item before shipping of the
item.(CICI-China-86-18328503374)
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.
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