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Easy Med Instrument Co., Ltd.

FDA Regulatory Profile

Easy Med Instrument Co., Ltd. appears in FDA public data with 0 recalls, 4 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on May 13, 2016.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K153045SunStim Peripheral Nerve Stimulator/Sunstim Plus Peripheral Nerve StimulatorMay 13, 2016
K143430SmartTENSMay 29, 2015
K050921EASYSTIM NMS-28December 12, 2005
K040253EASY MED TN-28 CApril 8, 2004

FDA data resources