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Goodman Co., Ltd.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
2
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K243944Aperta NSE PTA Balloon Dilatation CatheterApril 22, 2025
K232013Aperta NSE PTA Balloon Dilatation Catheter (AW18-05040040/AA18-05040040, AW18-09040040/AA18-09040040March 28, 2024
K010763GOODNETMay 25, 2001