Medical Device Manufacturer · US , Mchenry , IL

Analogic Corp. - FDA 510(k) Cleared Devices

32 submissions · 32 cleared · Since 1981

32

Total

32

Cleared

0

Denied

FDA 510(k) Regulatory Record - Analogic Corp. Cardiovascular ✕

13 devices

1-13 of 13

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

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

Cardiovascular · 86d

Cleared Jan 21, 1983

Cardiovascular · 17d

Cleared Oct 18, 1982

SIEMENS SIRECUST SYSTEM

Cardiovascular · 95d

Cleared Jan 22, 1981

SIRECUST 400 SYSTEM PATIENT MONITORING

Cardiovascular · 141d