Qingdao Hisense Medical Equipment Co., Ltd.

FDA Regulatory Profile

Qingdao Hisense Medical Equipment Co., Ltd. appears in FDA public data with 0 recalls, 9 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on May 16, 2024.

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Summary

Total Recalls
0
510(k) Clearances
9
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K233841HD80 Series Ultrasound Diagnostic SystemMay 16, 2024
K233439HD60 Series Ultrasound Diagnostic SystemFeb 21, 2024
K222208Hisense LCD monitor HMD2C21A, HMD4C27S, HMD6C30DNov 17, 2022
K222132Hisense LCD monitor HMD2G21S, HMD3G21SNov 8, 2022
K221567LCD monitor (HMD3C21S), LCD monitor (HMD5G21S)Jul 26, 2022
K213862HD60 Series Ultrasound Diagnostic SystemJun 8, 2022
K160347Hisense LDC monitor models HMD2G21/HMD3G21/HMD5G21Mar 3, 2016
K152030Hisense 2MP/3MP LCD Monitor (HMD2C21/HMD3C21)Sep 16, 2015
K151709Hi-Light Diagnostic Ultrasound SystemsJul 17, 2015