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Medicore Co., Ltd.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K212412IRIS-XPSeptember 13, 2021
K110374MAX PULSE SYSTEMJune 13, 2011
K073323SA-3000PNovember 29, 2007