Zhejiang Kangkang Medical-Devices Co., Ltd.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K213535Sterile Safety Hypodermic Needles for Single UseMay 13, 2022
K210229Sterile Auto-Disable Syringes with/without Needle for Single UseFebruary 15, 2022
K210232Sterile Hypodermic Needles for Single UseSeptember 23, 2021
K210227Sterile syringe for single use with/without needleSeptember 10, 2021