Shenzhen Ant Hi-Tech Industrial Co., Ltd.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K131770PRESSURE CONNECTING TUBEFebruary 26, 2014
K102648ANT INFLATION DEVICE/ANT INFLATION DEVICE COMPACT PACKJuly 1, 2011
K091408DISPOSABLE PRESSURE TRANSDUCERAugust 18, 2009
K072696ANT ANGIOGRAPHIC SYRINGES, MODEL(S) 100101,102,103,100201,202,203,204,100301,200101,201,202, 203,200May 2, 2008