We herehy delightedly announce that G1B Pulse Oximeter got FDA 510(K) approved. The clearance number is K082789. Link as below for 510(k) Premarket Notification Database:

http://www.accessdata.fda.gov/scrIpts/cdrh/cfdocs/cfPMN/pmn.cfm

Please enter the clearance number in the form,and you will find the detailed information.

Thanks for your concern all through. We assure you our strong support in our mutual-cooperation!