FDA 510(k) Applications Submitted by DIROS TECHNOLOGY, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K150371 02/13/2015 Diros OWL Sterile Single Use TridentTM R.F. Insulated Cannulae,Models DTR and DTRH DIROS TECHNOLOGY, INC.
K110593 03/02/2011 OWL RF PROBES DIROS TECHNOLOGY, INC.
K141586 06/13/2014 OWL CANNULAE DIROS TECHNOLOGY, INC.
K102566 09/07/2010 OWL CANNULAE DIROS TECHNOLOGY, INC.
K062758 09/15/2006 OWL URF-3AP DIROS TECHNOLOGY, INC.
K093185 10/09/2009 OWL UNIVERSAL RF SYSTEM URF-3AP (ML) DIROS TECHNOLOGY, INC.
K021869 06/06/2002 OWL RADIOFREQUENCY SYSTEM, MODEL URF-2AP DIROS TECHNOLOGY, INC.


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