FDA 510(k) Applications Submitted by APK TECHNOLOGY CO., LTD
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K082846 | 09/29/2008 | APK SPO2 PULSE OXIMETER SENSOR | APK TECHNOLOGY CO., LTD |
| K102825 | 09/29/2010 | BLOOD PRESSURE CUFF | APK TECHNOLOGY CO., LTD |
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