FDA 510(k) Applications Submitted by SHINICHI YAMANAKA
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K061302 |
05/10/2006 |
DIGITAL PRINTER P6000D SERIES, MODEL P6000DU |
MITSUBISHI ELECTRIC CORPORATION KYOTO WORKS |
| K051521 |
06/08/2005 |
REGIUS RS-1000, MEDICAL IMAGE PROCESSING WORKSTATION |
KONICA MINOLTA MEDICAL & GRAPHIC, INC. |
| K051523 |
06/08/2005 |
REGIUS CONSOLE CS-2000 AND REGIUS CONSOLE CS-3000, MEDICAL IMAGE PROCESSING WORKSTATION |
KONICA MINOLTA MEDICAL & GRAPHIC, INC. |
| K042133 |
08/09/2004 |
DRY LASER IMAGER, MODEL DRYPRO MODEL 793 |
KONICA MINOLTA MEDICAL & GRAPHIC, INC. |
| K032681 |
08/29/2003 |
KONICA LASER IMAGER, MODEL DRYPRO MODEL 771 |
KONICA MEDICAL AND GRAPHIC CORPORATION |
| K042386 |
09/02/2004 |
DIRECT DIGITIZER, REGIUS MODEL 190 |
KONICA MINOLTA MEDICAL & GRAPHIC, INC. |
| K053173 |
11/14/2005 |
DS CASSETTE |
KONICA MINOLTA MEDICAL & GRAPHIC, INC. |
| K053444 |
12/09/2005 |
KOWA KT-800 |
KOWA CO. LTD. |
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