FDA 510(k) Applications Submitted by DONALD J SHERRATT
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. |
K070829 |
03/26/2007 |
SYNEPIX 4600 DETECTOR |
ANALOGIC CORPORATION |
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. |
K052136 |
08/05/2005 |
GR17 DIGITAL DETECTOR |
ANRAD CORP. |
K042821 |
10/12/2004 |
DIGITAL DETECTOR, MODEL GR17 |
ANRAD CORP. |
K043025 |
11/03/2004 |
SYNERAD OMNI, DIGITAL X-RAY SYSTEM, MODEL AN6250 |
ANALOGIC CORP. |
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