Analogic Corp. - FDA 510(k) Cleared Devices
Recent clearances: SYNERAD OMNI, MODELS AN6255 AND AN6265, SYNERAD IMPACT 60, SYNERAD IMPACT 72 AND ANALOGIC AMS1600, LIFEGARD II FAMILY MULTI-FUNCTION PATIENT MONITOR, MODELS AN4320, AN4320P, AN4321P, AN4322P & AN3423P
32
Total
32
Cleared
0
Denied
FDA 510(k) Regulatory Record - Analogic Corp. Cardiovascular ✕
13 devices
Cleared
Jun 14, 2005
LIFEGARD II FAMILY MULTI-FUNCTION PATIENT MONITOR, MODELS AN4320, AN4320P,...
Cardiovascular
63d
Cleared
Aug 06, 2004
C3 AND LIFEGARD ICG IMPEDANCE CARDIOGRAPHY MONITORS
Cardiovascular
70d
Cleared
Jul 20, 2004
C1 SERIES PATIENT MONITOR, MODELS 863051, 863052, 863053, 863054
Cardiovascular
57d
Cleared
May 09, 2003
C3 PATIENT MONITOR
Cardiovascular
45d
Cleared
Aug 20, 1998
NPB3900 SERIES PATIENT MONITORS
Cardiovascular
198d
Cleared
Dec 20, 1996
NPB-4000
Cardiovascular
179d
Cleared
Oct 16, 1986
PATIENT MON 1280/1281/120C/121C & MULTI-PARA CART
Cardiovascular
238d
Cleared
Jul 15, 1986
SIEMENS SIRECUST MODELS 403P,403-2P & 403N
Cardiovascular
204d
Cleared
Apr 10, 1985
SYSTEM SIRECUST 400 SIEMENS SIRECUST 456-1A
Cardiovascular
121d
Cleared
Mar 31, 1983
SIRECUST 400
Cardiovascular
86d
Cleared
Jan 21, 1983
SIRECUST 456
Cardiovascular
17d
Cleared
Oct 18, 1982
SIEMENS SIRECUST SYSTEM
Cardiovascular
95d