FDA 510(k) Applications Submitted by RICHARD P BENNETT
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K030668 |
03/03/2003 |
MODEL 3100 WRISTOX PULSE OXIMETER |
NONIN MEDICAL, INC. |
K001085 |
04/04/2000 |
MODIFICATION TO ONYX, FINGER CLIP PULSE OXIMETER, MODEL 9500 |
NONIN MEDICAL, INC. |
K031487 |
05/12/2003 |
MODEL AVANT 2120 PULSE OXIMETER AND NIBP |
NONIN MEDICAL, INC. |
K001930 |
06/26/2000 |
MODEL 8500, HAND HELD PULSE OXIMETER, MODEL 8500 |
NONIN MEDICAL, INC. |
K982969 |
08/25/1998 |
NONIN PULSE OXIMETER AND CARBON DIOXIDE DETECTOR, MODELS 9843, 9845 AND 9847 |
NONIN MEDICAL, INC. |
K002690 |
08/29/2000 |
MODEL 2500, PALMSAT HAND HELD PULSE OXIMETER, MODEL 2500 |
NONIN MEDICAL, INC. |
K023044 |
09/12/2002 |
MODEL 9600, AVANT PULSE OXIMETER |
NONIN MEDICAL, INC. |
K013319 |
10/05/2001 |
NONIN MODEL 2120 PULSE OXIMETER AND NONINVASIVE BLOOD PRESSURE (NIBP) MONITOR |
NONIN MEDICAL, INC. |
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