FDA 510(k) Applications Submitted by AGFA CORP.

FDA 510(k) Number Submission Date Device Name Applicant
K022292 07/15/2002 IMPAX DIAGNOSTIC DISPLAY STATION,IMPAX CLINICAL REVIEW STATION,IMPAX FOR CARDIOLOGY CLINICAL REVIEW SATATION,IMPAX ORTHO AGFA CORP.
K021542 05/10/2002 ADC DENTAL AGFA CORP.
K022658 08/09/2002 LR DICOM CONTROLLER AGFA CORP.
K032635 08/26/2003 DRYSTAR 5300 MEDICAL IMAGE PRINTER, MODEL 5300 AGFA CORP.
K023287 10/02/2002 DRYSTAR 5500 AGFA CORP.
K050810 03/31/2005 AGFA CR50.0 AGFA CORP.
K041701 06/22/2004 AFGA CR25.0 COMPUTED RADIOGRAPHY SYSTEM AGFA CORP.
K042779 10/06/2004 RADIOTHERAPY SOLUTION BASED ON CR AGFA CORP.
K063421 11/13/2006 DX-SI AGFA CORP.
K023020 09/11/2002 AGFA MAMORAY MAMMOGRAPHIC CASSETTE, AGFA METAL-BODIED CAWO CASSETTE, AGFA CURIX AND LIGHTWEIGHT CASSETTE AGFA CORP.
K040344 02/12/2004 IMPAX OT3000 ORTHOPEDIC WORKSTATION AGFA CORP.
K040555 03/02/2004 IMPAX CLIENT EMBRACE AGFA CORP.
K050751 03/23/2005 IMPAX ORTHOPAEDIC WORKSTATION, MODEL IMPAX ES 5.X AGFA CORP.
K053458 12/13/2005 WEB1000 AGFA CORP.
K010571 02/26/2001 ADC QS/IPD WORKSTATION AGFA CORP.
K012750 08/16/2001 ADC PEDIATRIC AGFA CORP.
K012941 08/31/2001 DRYSTAR, MODEL 4500M AGFA CORP.
K012010 06/27/2001 MODIFICATION TO LR 5200 FILM RECORDER AGFA CORP.
K000159 01/19/2000 AGFA DIAGNOSTIC CENTER ADC, ADC COMPACT, AND ADC SOLO AGFA CORP.


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