FINGERTIP PULSE OXIMETER, MODEL MD300I


Device Classification Name

oximeter

510(k) Number K072825
Device Name FINGERTIP PULSE OXIMETER, MODEL MD300I
Applicant
BEIJING CHOICE ELECTRONIC TECHNOLOLGY CO., LTD.
suite 8d, zhongxin zhongshan
no19, ln999, zhong shan nan er
shanghai, 

CN

200030

Applicant Contact diana hong
Correspondent
BEIJING CHOICE ELECTRONIC TECHNOLOLGY CO., LTD.
suite 8d, zhongxin zhongshan
no19, ln999, zhong shan nan er
shanghai, 

CN

200030

Correspodent Contact diana hong
Regulation Number 870.2700
Classification Product Code
DQA  
Date Received 10/02/2007
Decision Date 01/14/2008
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Cardiovascular

510k Review Panel

Anesthesiology

summary

summary

Type Special
Reviewed by Third Party No

Combination Product

No