FDA 510(k) Applications Submitted by KOJI KUBO
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K111103 |
04/20/2011 |
DIGITAL X-RAY IMAGING SYSTEM |
RF CO., LTD |
| K071384 |
05/17/2007 |
MODIFICATION TO: DIGITAL BLOOD PRESSURE MONITOR, MODEL 1901 |
NIHON SEIMITSU SOKKI CO., LTD. |
| K111612 |
06/09/2011 |
DIGITAL RETINAL CAMERA |
CANON, INC. |
| K071596 |
06/12/2007 |
POTABLE AIR MASSAGER PUTIFINO, MODEL AM-7 |
NIHON SEIMITSU SOKKI CO., LTD. |
| K111682 |
06/15/2011 |
DIGITAL RADIOGRAPHY |
CANON, INC.-MEDICAL EQUIPMENT GROUP |
| K111710 |
06/20/2011 |
FULL AUTO TONOMETER MODEL TX-20 |
CANON, INC.-MEDICAL EQUIPMENT GROUP |
| K102012 |
07/16/2010 |
DIGITAL RADIOGRAPHY |
CANON, INC.-MEDICAL EQUIPMENT GROUP |
| K102013 |
07/16/2010 |
DIGITAL RETINAL CAMERA |
CANON, INC.-MEDICAL EQUIPMENT GROUP |
| K092389 |
08/05/2009 |
DISPOSAL ECG ELECTRODES, MODEL EASYRODE |
SUZUKEN CO., LTD. |
| K112309 |
08/11/2011 |
DIGITAL RADIOGRAPHY |
CANON, INC.-MEDICAL EQUIPMENT GROUP |
| K112620 |
09/08/2011 |
DISITAL BLOOD PRESSURE MONITOR |
NIHON SEIMITSU SOKKI CO., LTD. |
| K013054 |
09/11/2001 |
KONICA DIRECT DIGITIZER REGIUS MODEL 350 |
KONICA MINOLTA MEDICAL & GRAPHIC, INC. |
| K112690 |
09/15/2011 |
BLOOD PRESSURE MONITOR |
NIHON SEIMITSU SOKKI CO., LTD. |
| K112691 |
09/15/2011 |
BLOOD PRESSURE MONITOR |
NIHON SEIMITSU SOKKI CO., LTD. |
| K023061 |
09/16/2002 |
KONICA DIRECT DIGITIZER REGIUS, MODEL 170 |
KONICA MINOLTA MEDICAL & GRAPHIC, INC. |
| K093102 |
10/01/2009 |
AMBULATORY BLOOD PRESSURE MONITOR, MODELS FB-270 AND DS-270 |
NIHON SEIMITSU SOKKI CO., LTD. |
| K073087 |
11/01/2007 |
NON-CONTACT TONOMETER, MODEL FT-1000 |
TOMEY CORPORATION |
| K103591 |
12/07/2010 |
DIGITAL RADIOGRAPHY |
CANON, INC.-MEDICAL EQUIPMENT GROUP |
| K013052 |
09/11/2001 |
KONICA LASER IMAGER, DRYPRO MODEL 751/752 |
KONICA MINOLTA MEDICAL & GRAPHIC, INC. |
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