Shandong Lianfa Medical Plastic Products Co. , Ltd.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K222472Lancing System, Sterile Lancet for Single Use, Lancing DeviceNovember 30, 2022
K222376Lianfa Safety Lancet (Five Models: NPA, PA, PA2, TPA, and APA)October 3, 2022