Analogic Corp. - FDA 510(k) Cleared Devices
32
Total
32
Cleared
0
Denied
32 devices
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 22, 1984
PATIENT MONITOR #404
Anesthesiology
335d
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
Cleared
Jan 22, 1981
SIRECUST 400 SYSTEM PATIENT MONITORING
Cardiovascular
141d