Tianjin Medis Medical Device Co., Ltd.

FDA Regulatory Profile

Tianjin Medis Medical Device Co., Ltd. appears in FDA public data with 0 recalls, 3 510(k) clearances, 4 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on July 30, 2019.

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
4
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K190274Endotracheal TubeJuly 30, 2019
K182548Accucuff Cuff Pressure IndicatorJanuary 25, 2019
K160694Disposable Endotracheal tube, sterile, AccuCuffApril 7, 2017