The following data is part of a premarket notification filed by Apk Technology Co., Ltd with the FDA for Apk Spo2 Pulse Oximeter Sensor.
| Device ID | K082846 |
| 510k Number | K082846 |
| Device Name: | APK SPO2 PULSE OXIMETER SENSOR |
| Classification | Oximeter |
| Applicant | APK TECHNOLOGY CO., LTD SUITE 8D, NO19, ZHONGSHAN MANSION, LANE 999, ZHONGSHAN No. 2 Road(s); Shanghai, CN 200030 |
| Contact | Diana Hong |
| Correspondent | Diana Hong APK TECHNOLOGY CO., LTD SUITE 8D, NO19, ZHONGSHAN MANSION, LANE 999, ZHONGSHAN No. 2 Road(s); Shanghai, CN 200030 |
| Product Code | DQA |
| CFR Regulation Number | 870.2700 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2008-09-29 |
| Decision Date | 2009-04-03 |
| Summary: | summary |