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 |