ClearanceBrief
Company ยท CN

APK Technology Co., Ltd.

FDA 510(k) clearances and medical device recalls filed under this name, 1991 to 2025. Name variants (Inc, Corp, punctuation) are merged.

7510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
DQAOximeter2
LRPTray, Surgical2
DSACable, Transducer And Electrode, Patient, (Including Connector)1
DXQBlood Pressure Cuff1
FTCLight, Ultraviolet, Dermatological1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Apr 7, 2025K250425Ultraviolet Phototherapy Device
APK Technology Co., Ltd., CN
FTC
Jun 8, 2018K172981Reusable SpO2 Sensors, Disposable SpO2 Sensors
APK Technology Co., Ltd., CN
DQA
Apr 24, 2017K170536ECG Disposable Lead Wire
APK Technology Co., Ltd., CN
DSA
Mar 2, 2011K102825BLOOD PRESSURE CUFF
APK Technology Co., Ltd., CN
DXQ
Apr 3, 2009K082846APK SPO2 PULSE OXIMETER SENSOR
APK Technology Co., Ltd., CN
DQA
Jul 29, 1991K903963KITS AND TRAYS FOR ONE TIME USE ONLY
Apk Technology, IL
LRP
Jul 29, 1991K903962INSTRUMENTS FOR ONE TIME USE/ DISPOSABLE
Apk Technology, IL
LRP

Latest recalls

DateFirm and productCodeLinked 510(k)
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