FDA 510(k) Applications Submitted by ANALOGIC CORP.
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K050919 |
04/12/2005 |
LIFEGARD II FAMILY MULTI-FUNCTION PATIENT MONITOR, MODELS AN4320, AN4320P, AN4321P, AN4322P & AN3423P |
ANALOGIC CORP. |
K052447 |
09/07/2005 |
SYNERAD IMPACT 60, SYNERAD IMPACT 72 AND ANALOGIC AMS1600 |
ANALOGIC CORP. |
K040995 |
04/16/2004 |
SYNERAD MULTI DIGITAL X-RAY SYSTEM, MODEL AN6150 |
ANALOGIC CORP. |
K071430 |
05/23/2007 |
SYNERAD OMNI, MODELS AN6255 AND AN6265 |
ANALOGIC CORP. |
K041376 |
05/24/2004 |
C1 SERIES PATIENT MONITOR, MODELS 863051, 863052, 863053, 863054; OPTIONAL PRINTER FOR CI, MODEL M3925A |
ANALOGIC CORP. |
K041434 |
05/28/2004 |
C3 AND LIFEGARD ICG IMPEDANCE CARDIOGRAPHY MONITORS |
ANALOGIC CORP. |
K043025 |
11/03/2004 |
SYNERAD OMNI, DIGITAL X-RAY SYSTEM, MODEL AN6250 |
ANALOGIC CORP. |
K991626 |
05/11/1999 |
WEBRAD COMPUTED RADIOGRAPHY QUALITY ASSURANCE WORKSTATION |
ANALOGIC CORP. |
K962424 |
06/24/1996 |
NPB-4000 |
ANALOGIC CORP. |
K964890 |
12/06/1996 |
ANATOM 2000 |
ANALOGIC CORP. |
K030931 |
03/25/2003 |
C3 PATIENT MONITOR |
ANALOGIC CORP. |
K033345 |
10/20/2003 |
AN5150 AND AN7150 DIGITAL RADIOLOGY SYSTEMS |
ANALOGIC CORP. |
K001336 |
04/27/2000 |
DR9000 DIGITAL RADIOGRAPHY X-RAY SYSTEM |
ANALOGIC CORP. |
K001341 |
04/27/2000 |
DR5000 DEDICATED CHEST X-RAY SYSTEM |
ANALOGIC CORP. |
K974455 |
11/25/1997 |
ANATOM 1000 (A MINUS, A-) |
ANALOGIC CORP. |
K980168 |
01/16/1998 |
COMPUTED RADIOGRAPHY QUALITY ASSURANCE SOFTWARE |
ANALOGIC CORP. |
K983395 |
09/25/1998 |
FETALGARD 3000 FETAL MONITOR |
ANALOGIC CORP. |
K980411 |
02/03/1998 |
NPB3900 SERIES PATIENT MONITORS |
ANALOGIC CORP. |
K011304 |
04/30/2001 |
OB-1 FETAL MONITOR |
ANALOGIC CORP. |
K002503 |
08/14/2000 |
FETALGARD LITE |
ANALOGIC CORP. |
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