Agfa Corp. - FDA 510(k) Cleared Devices
19
Total
19
Cleared
0
Denied
Agfa Corp. has 19 FDA 510(k) cleared radiology devices. Based in Greenville, US.
Historical record: 19 cleared submissions from 2000 to 2006.
Browse the complete list of FDA 510(k) cleared radiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
19 devices
Cleared
Nov 22, 2006
DX-SI
Radiology
9d
Cleared
Dec 22, 2005
WEB1000
Radiology
9d
Cleared
Apr 21, 2005
IMPAX ORTHOPAEDIC WORKSTATION, MODEL IMPAX ES 5.X
Radiology
29d
Cleared
Apr 21, 2005
AGFA CR50.0
Radiology
21d
Cleared
Oct 21, 2004
RADIOTHERAPY SOLUTION BASED ON CR
Radiology
15d
Cleared
Jul 22, 2004
AFGA CR25.0 COMPUTED RADIOGRAPHY SYSTEM
Radiology
30d
Cleared
May 26, 2004
IMPAX CLIENT EMBRACE
Radiology
85d
Cleared
May 12, 2004
IMPAX OT3000 ORTHOPEDIC WORKSTATION
Radiology
90d
Cleared
Sep 24, 2003
DRYSTAR 5300 MEDICAL IMAGE PRINTER, MODEL 5300
Radiology
29d
Cleared
Oct 22, 2002
DRYSTAR 5500
Radiology
20d
Cleared
Sep 26, 2002
AGFA MAMORAY MAMMOGRAPHIC CASSETTE, AGFA METAL-BODIED CAWO CASSETTE, AGFA...
Radiology
15d
Cleared
Sep 12, 2002
IMPAX DIAGNOSTIC DISPLAY STATION,IMPAX CLINICAL REVIEW STATION,IMPAX FOR...
Radiology
59d
Cleared
Sep 06, 2002
LR DICOM CONTROLLER
Radiology
28d
Cleared
Aug 06, 2002
ADC DENTAL
Radiology
88d
Cleared
Nov 29, 2001
DRYSTAR, MODEL 4500M
Radiology
90d
Cleared
Nov 14, 2001
ADC PEDIATRIC
Radiology
90d
Cleared
Sep 20, 2001
MODIFICATION TO LR 5200 FILM RECORDER
Radiology
85d
Cleared
Mar 28, 2001
ADC QS/IPD WORKSTATION
Radiology
30d
Cleared
Feb 16, 2000
AGFA DIAGNOSTIC CENTER ADC, ADC COMPACT, AND ADC SOLO
Radiology
28d