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. Obstetrics & Gynecology ✕
5 devices
Cleared
May 29, 2001
OB-1 FETAL MONITOR
Obstetrics & Gynecology
29d
Cleared
Nov 09, 2000
FETALGARD LITE
Obstetrics & Gynecology
87d
Cleared
Aug 12, 1999
FETALGARD 3000 FETAL MONITOR
Obstetrics & Gynecology
321d
Cleared
May 15, 1995
FETALGARD 3000 - MODELS IP1, IP2, AP2 AND AP3
Obstetrics & Gynecology
104d
Cleared
Jul 22, 1991
FETALGARD 2000
Obstetrics & Gynecology
188d