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Gostar Co., Ltd.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K241843TD-7301 Spirometer (TD-7301)November 20, 2024
K222810TD-7301 Peak Flow meterDecember 19, 2023
K221419TD-5010 Lancing Device and TD-5084 Sterile LancetsJanuary 20, 2023