FDA 510(k) Applications Submitted by LORI ROTH

FDA 510(k) Number Submission Date Device Name Applicant
K050056 01/11/2005 MODEL 2500A PALMSAT PULSE OXIMETER NONIN MEDICAL, INC.
K092101 07/14/2009 REUSABLE PULSE OXIMETER SENSOR, MODEL 8000 SERIES NONIN MEDICAL, INC.
K052829 10/05/2005 WRISTOX MODEL 3100 PULSE OXIMETER NONIN MEDICAL, INC.
K093306 10/22/2009 SINGLE-PATIENT USE DISPOSABLE SENSOR NONIN MEDICAL, INC.
K093853 12/16/2009 SINGLE-PATIENT USE DISPOSABLE SENSOR SERIES NONIN MEDICAL, INC.
K080255 01/31/2008 NONIN MEDICAL, INC., MODEL 7500 DIGITAL PULSE OXIMETER NONIN MEDICAL, INC.
K090807 03/25/2009 REGIONAL OXIMETER SYSTEM, MODEL 7600 NONIN MEDICAL, INC.
K051107 05/02/2005 ONYX II FINGER PULSE OXIMETER, MODEL 9550 NONIN MEDICAL, INC.
K081285 05/06/2008 FINGER PULSE OXIMETER, MODEL 9560 NONIN MEDICAL, INC.
K071285 05/07/2007 DIGITAL PULSE OXIMETER, MODEL 7500 NONIN MEDICAL, INC.
K071415 05/21/2007 DIGITAL PULSE OXIMETER, MODEL 7500FO NONIN MEDICAL, INC.
K092678 09/01/2009 EVISION DATA MANAGEMENT SOFTWARE NONIN MEDICAL, INC.
K052669 09/27/2005 AVANT DIGITAL PULSE OXIMETRY SYSTEM, MODEL 4000, 4100 NONIN MEDICAL, INC.
K053130 11/08/2005 ONYX II FINGER PULSE OXIMETER, MODEL 9550 NONIN MEDICAL, INC.
K063752 12/19/2006 LIFESENSE, MODEL LS1-9R NONIN MEDICAL, INC.


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