FDA 510(k) Applications Submitted by MARY MOORE
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K150221 |
01/30/2015 |
EPX-4440HD and EPX-4400HD with FICE |
FUJIFILM MEDICAL SYSTEM U.S.A., INC. |
| K151474 |
06/01/2015 |
Fujifilm Diathermic Slitter (FlushKnife), Diathermic Slitter (ClutchCutter) |
FUJIFILM MEDICAL SYSTEM U.S.A., INC. |
| K142629 |
09/16/2014 |
EG-530CT, EG-530D, EC-530DL, and ES-530WE Endoscopes |
FUJIFILM MEDICAL SYSTEM U.S.A., INC. |
| K143556 |
12/15/2014 |
Fujifilm Double Balloon Endoscopes Models EN-530T and EN-580T |
FUJIFILM MEDICAL SYSTEMS U.S.A., INC. |
| K143732 |
12/29/2014 |
FUJIFILM Endoscope Models EC-600HL and EC-600LS |
FUJIFILM Medical Systems U.S.A., Inc. |
| K140149 |
01/22/2014 |
EPX-4440HD DIGITAL VIDEO PROCESSOR |
FUJIFILM MEDICAL SYSTEMS U.S.A., INC. |
| K101757 |
06/23/2010 |
SONOSITE NANOMAXX SERIES ULTRASOUND SYSTEM, SONOSITE MAXX SERIES ULTRASOUND SYSTEM |
SONOSITE,INC. |
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