The following data is part of a premarket notification filed by Beijing Choice Electronic Technololgy Co., Ltd. with the FDA for Fingertip Pulse Oximeter, Model Md300i.
| Device ID | K072825 |
| 510k Number | K072825 |
| Device Name: | FINGERTIP PULSE OXIMETER, MODEL MD300I |
| Classification | Oximeter |
| Applicant | BEIJING CHOICE ELECTRONIC TECHNOLOLGY CO., LTD. SUITE 8D, ZHONGXIN ZHONGSHAN NO19, LN999, ZHONG SHAN NAN ER Shanghai, CN 200030 |
| Contact | Diana Hong |
| Correspondent | Diana Hong BEIJING CHOICE ELECTRONIC TECHNOLOLGY CO., LTD. SUITE 8D, ZHONGXIN ZHONGSHAN NO19, LN999, ZHONG SHAN NAN ER Shanghai, CN 200030 |
| Product Code | DQA |
| CFR Regulation Number | 870.2700 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2007-10-02 |
| Decision Date | 2008-01-14 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00851440007001 | K072825 | 000 |