Atlas FDA

MODIFICATION TO: CIC PRO CLINICAL INFORMATION CENTER CENTRAL STATION

FDA 510(k) clearance K053356 · decided 2006-04-19

Clearance details

K-number
K053356
Device name
MODIFICATION TO: CIC PRO CLINICAL INFORMATION CENTER CENTRAL STATION
Applicant
Ge Medical Systems Information Technologies
Decision
Substantially Equivalent
Date received
2005-12-02
Decision date
2006-04-19
Days to decision
138 days
Clearance type
Traditional
Product code
DXJ
Device class
2
Regulation number
870.2450
Medical specialty
Cardiovascular
Advisory committee
Cardiovascular
Location
Milwaukee, WI, US
Third-party review
No
Expedited review
No

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Recalls involving this device

RecordFirmDate
GE Healthcare CIC Pro" Software Versions 5.0.3, 5.0.6 ,5.0.7, 5.0.8 and 4.1. The CIC Pro" recall (Z-1232-2009)GE Medical Systems Information Tecnology2009-05-04

PMA approvals by this applicant

RecordFirmDate
COROMETRICS MODEL 120 F-SERIES MATERNAL/FETAL MONITOR WITH INTERGRATED FETAL OXYGEN SATURATION MONITORING (P000016/S002)Ge Medical Systems Information Technologies2003-10-15
COROMETRICS MODEL 120 SERIES MATERNAL/FETAL MONITOR W/INTEGRATED FETAL PULSE OXIMETRY (P000016/S001)Ge Medical Systems Information Technologies2001-11-09
COROMETRICS 120F SERIES MATERNAL/FETAL MONITOR (P000016)Ge Medical Systems Information Technologies2001-02-09
MODEL 515 NEONATAL MONIOTR (P840037/S001)Ge Medical Systems Information Technologies1986-11-19