Wenzhou Longwan Medical Device Factory

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
1
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K240165Aneroid Sphygmomanometer with Stethoscope; Aneroid SphygmomanometerMarch 20, 2024