Diros Technology, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
8
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K170708OWL RF INSULATED CANNULAEJune 27, 2017
K150371Diros OWL Sterile Single Use TridentTM R.F. Insulated Cannulae,Models DTR and DTRHJuly 30, 2015
K141586OWL CANNULAEDecember 30, 2014
K102566OWL CANNULAEJune 3, 2011
K110593OWL RF PROBESMay 5, 2011
K093185OWL UNIVERSAL RF SYSTEM URF-3AP (ML)January 22, 2010
K062758OWL URF-3APSeptember 27, 2006
K021869OWL RADIOFREQUENCY SYSTEM, MODEL URF-2APJuly 1, 2002