FDA 510(k) Applications Submitted by SHEILA DRISCOLL

FDA 510(k) Number Submission Date Device Name Applicant
K060433 02/21/2006 DIGITAL RADIOGRAPHY CXDI-50C CANON INC.
K090466 02/21/2009 DIGITAL RETINAL CAMERA, CR-1 MARK II CANON, INC.
K090623 03/09/2009 DIGITAL RADIOGRAPHY CXDI-40G COMPACT CANON U.S.A., INC.
K080883 03/31/2008 CR-1 CANON, INC.
K050987 04/19/2005 DIGITAL RADIOGRAPHY MODEL CXDI-40EG CANON, INC.
K031447 05/07/2003 CANON, DIGITAL RADIOGRAPHY, MODEL CXDI-50G CANON INC.
K091435 05/14/2009 DIGITAL RADIOGRAPHY MODEL CXDI-55G CANON INC.
K091436 05/14/2009 DIGITAL RADIOGRAPHY, MODEL CXDI-55C CANON, 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.
K091545 05/27/2009 DIGITAL RADIOGRAPHY CXDI-60C CANON INC.
K041546 06/09/2004 DIGITAL FUNDUS CAMERA, MODEL CF-60DSI CANON INC.
K081648 06/12/2008 DIGITAL RADIOGRAPHY CXDI-60G CANON, INC.
K062221 08/02/2006 CXDI-40EC CANON, INC.
K092565 08/20/2009 DIGITAL RETINAL CAMERA CX-1 CANON COMPONENTS, INC.
K023750 11/08/2002 CANNON DIGITAL RADIOGRAPHY MODEL CXDI-40G CANON U.S.A., INC.
K023816 11/15/2002 CANON FULL AUTO TONOMETER TX-F CANON, INC.-UTSUNOMIYA OPTICAL PRODUCTS OPERATION
K003689 11/30/2000 CANON X-RAY DIGITAL CAMERA, MODEL CXDI-31 CANON U.S.A., INC.
K063717 12/14/2006 CF-1 CANON, INC.


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