FDA 510(k) Applications Submitted by CANON U.S.A., INC.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K980246 |
01/23/1998 |
NON-MYDRIATIC RETINAL CAMERA, MODEL CR6-45NM |
CANON U.S.A., INC. |
| K981556 |
05/01/1998 |
CANON X-RAY DIGITAL CAMERA CXDI-11 |
CANON U.S.A., INC. |
| K963079 |
08/07/1996 |
CANON TX-10 TONOMETER |
CANON U.S.A., INC. |
| K992547 |
07/30/1999 |
CANON X-RAY DIGITAL CAMERA, MODEL CXDI-22 |
CANON U.S.A., INC. |
| K992606 |
08/03/1999 |
CANON LASER BLOOD FLOWMETER (CLBF) MODEL 100 |
CANON U.S.A., INC. |
| K033624 |
11/18/2003 |
PACS SOFTWARE SOLUTION 2003 |
CANON U.S.A., INC. |
| K090623 |
03/09/2009 |
DIGITAL RADIOGRAPHY CXDI-40G COMPACT |
CANON U.S.A., INC. |
| K031629 |
05/27/2003 |
CANON NON-MYDRIATIC RETINAL CAMERA, MODEL CR-DGI |
CANON U.S.A., INC. |
| K031633 |
05/27/2003 |
CANON INC., DIGITAL RADIOGRAPHY, MODEL CXDI-40C |
CANON U.S.A., INC. |
| K023750 |
11/08/2002 |
CANNON DIGITAL RADIOGRAPHY MODEL CXDI-40G |
CANON U.S.A., INC. |
| K003689 |
11/30/2000 |
CANON X-RAY DIGITAL CAMERA, MODEL CXDI-31 |
CANON U.S.A., INC. |
| K023586 |
10/25/2002 |
DR-ER VERFSION OF CANON X-RAY DIGITAL CAMERAS |
CANON U.S.A., INC. |
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