Home / Companies / Smiths Medical

Smiths Medical

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K181660Acapella Choice Blue Vibratory PEP DeviceOctober 24, 2019
K050166PORTEX EMERGENCY CRICOTHYROIDOTOMY KITMay 26, 2005
K041348PORTEX ULTRAPERC PERCUTANEOUS DILATION TRACHEOSTOMY KIT_WITH SERIAL DILATORS OR SINGLE STAGE DILATORJuly 13, 2004