510(k) Report

510(k) · Cleared

Recalled · Class II · 2019

Cic Pro Clinical Information Center Central Station

K032370510(k) SpecialCleared Aug 13, 200312-day reviewClass II21 CFR 870.1025Recalls 5

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Ge Medical Systems Information Technologies · DSI Detector And Alarm, Arrhythmia

Cleared on Aug 13, 2003 as substantially equivalent to K001112 (General Electric Medical Systems Information Techn, 2000) after a 12-day review. Its family tree reaches back 1 generation to 2000. 23 later devices descend from it. It has been recalled 5 times.

Decided
Aug 13, 2003
Review
12 days
Class
Class II
Product code
DSI
Recalls
5
Predicates
1

Its longest line of descent runs back 1 generation to K001112 (2000). 23 later devices descend from it, 1 citing it directly.

Descendants, by year cleared 2006: 1 descendant cleared2007: 2 descendants cleared2014: 2 descendants cleared2008: 1 descendant cleared2010: 1 descendant cleared2011: 3 descendants cleared2016: 3 descendants cleared2018: 2 descendants cleared2020: 3 descendants cleared2025: 2 descendants cleared2024: 2 descendants cleared2022: 1 descendant clearedK001112 · GE Marquette Clinical Information Center, GE Marquette Cic · General Electric Medical Systems Information Techn · 2000200020052010201520202025
Descendants, by generation 1 generation forward: 1 descendant2 generations forward: 2 descendants3 generations forward: 3 descendants4 generations forward: 5 descendants5 generations forward: 4 descendants6 generations forward: 5 descendants7 generations forward: 3 descendants K001112 · GE Marquette Clinical Information Center, GE Marquette Cic · General Electric Medical Systems Information Techn · 20000+5
  1. Root · 1 generation backK001112 GE Marquette Clinical Information Center, GE Marquette CicGeneral Electric Medical Systems Information Techn · 2000
  2. This deviceK032370 Cic Pro Clinical Information Center Central StationGe Medical Systems Information Technologies · 2003
  3. Descendant · cites it directly · 22 of its ownK053356 Modification to: Cic Pro Clinical Information Center Central StationGe Medical Systems Information Technologies · 2006 · Recalled
  4. Descendant · 2 generations on · 10 of its ownK073372 Electrophysiology Systems Integrator (Epsi)Systemsone · 2007
  5. Descendant · 2 generations on · 10 of its ownK062976 Modification to Cic Pro Clinical Information CenterGe Medical Systems Information Technologies · 2007 · Recalled
  6. Descendant · 3 generations on · 9 of its ownK133882 Carescape Central Station (Formally Known as Cic Pro)Ge Medical Systems Information Technologies, Inc. · 2014 · Recalled
  7. Descendant · 3 generations on · 9 of its ownK083321 Cardio-ViewCurlview Igt, LLC · 2008

Showing 5 of 23 descendants. See all descendants

Descendants cleared per year

2006: 12007: 22008: 12010: 12011: 32014: 22016: 32018: 22020: 32022: 12024: 22025: 2
2006high 3 (2011) · low 0 (2009)2026

Most influential descendants

Showing 5 of 23 · See all
  • K053356Modification to: Cic Pro Clinical Information Center Central StationGe Medical Systems Information Technologies · 2006 · cites it directly22descendants
  • K073372Electrophysiology Systems Integrator (Epsi)Systemsone · 2007 · 2 generations on10descendants
  • K062976Modification to Cic Pro Clinical Information CenterGe Medical Systems Information Technologies · 2007 · 2 generations on10descendants
  • K133882Carescape Central Station (Formally Known as Cic Pro)Ge Medical Systems Information Technologies, Inc. · 2014 · 3 generations on9descendants
  • K083321Cardio-ViewCurlview Igt, LLC · 2008 · 3 generations on9descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−1K001112GE Marquette Clinical Information Center, GE Marquette CicGeneral Electric Medical Systems Information Techn2000—
0 (this device)K032370Cic Pro Clinical Information Center Central StationGe Medical Systems Information Technologies2003—
+1K053356Modification to: Cic Pro Clinical Information Center Central StationGe Medical Systems Information Technologies20062
+2K073372Electrophysiology Systems Integrator (Epsi)Systemsone2007—
+2K062976Modification to Cic Pro Clinical Information CenterGe Medical Systems Information Technologies20074
+3K133882Carescape Central Station (Formally Known as Cic Pro)Ge Medical Systems Information Technologies, Inc.20141
+3K083321Cardio-ViewCurlview Igt, LLC2008—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200610
200720
200810
201010
201130
201420
201630
201820
202030
202210
202420
202520
FIG. 1 — Lineage of K032370, 2000–2025Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Get the monthly Device Review Tracker

Notable FDA decisions, review times and new Class I recalls. See an issue.

Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in DSI? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new DSI device

  1. #1 K243349 BodyGuardian Remote Monitoring System (BGRMS…score 13.1 · 9 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) Report

What was it cleared against? (1)

Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.

TypeNumberDeviceApplicantDecidedRecalls
*K001112GE Marquette Clinical Information Center, GE Marquette CicGeneral Electric Medical Systems Information Techn2000—

What descends from it? (23)

See all 23

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K053356Modification to: Cic Pro Clinical Information Center Central StationGe Medical Systems Information Technologies200622

Has anything in its family been recalled? (0 Class I)

Recalls of this device

DateClassRecallRoot causeReason
Nov 12, 2019Class IIZ-0726-2020Software in the Use EnvironmentWhen connected to the Mission Critical (MC) and /or Information Exchange (IX) networks, certain versions of the CARESCAPE Telemetry Server, ApexPro Telemetry Server, CARESCAPE Central Station (CSCS) version 1 and Central Information…
Feb 27, 2009Not classifiedZ-1232-2009Software designGE Healthcare is aware of potential network time issues associated with the time change aspects of certain CARESCAPE CIC Pro" software versions. These issues may impact patient safety. No reported patient injuries or illnesses for the use…
Jan 24, 2007Not classifiedZ-0280-2008Software designTwo separate issues may occur with operating The CiC Pro v4.1 System with Telemetry. 1) Experience a loss of audible alarms when operating system memory resource reaches approximately 170MG. This will occur if CIC Pro continuously runs…
Jan 24, 2007Not classifiedZ-0891-2007OtherAlarm and Reboot problems: Two separate issues could occur with the CIC Pro system when used with Telemetry. Each issue occurs in software version v4.1 only; A) the system may experience a loss of audible alarms when operating system…
Oct 11, 2004Not classifiedZ-0030-05OtherThe following two conditions may occur with the printing of full disclosure strips and reports, printing of the alarm history events stored on a GE Unity Network Patient Data Server (PDS), and printing of caliper reports in the GE CIC Pro…

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • Its one ancestor has no recall.
  • Of its descendants, K053356 (Ge Medical Systems Information Technologies, 2006) has gone furthest, with 22 descendants of its own.

How does its category compare?

All DSI devices

DSI Detector And Alarm, Arrhythmia: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · DSI

1in 2025

2007: 72008: 52009: 62010: 62011: 62012: 32013: 12014: 42015: 92016: 62018: 22019: 32020: 22023: 22024: 12025: 12026 (partial year): 1
2007high 9 (2015) · low 0 (2017)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · DSI

243in 2019

2007: 151 days median2008: 70 days median2009: 73 days median2010: 111 days median2011: 114 days median2012: 113 days median2014: 200 days median2015: 127 days median2016: 224 days median2019: 243 days median
2007high 243 (2019) · low 70 (2008)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · DSI

18in 2025

2007: 42008: 82009: 32010: 52011: 32012: 12018: 12019: 42020: 22022: 12023: 22025: 182026 (partial year): 1
2007high 18 (2025) · low 0 (2013)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · DSI

712in 2025

2007: 642008: 1562009: 2792010: 8232011: 7932012: 7662013: 7952014: 1,0002015: 1,6452016: 4,3522017: 3,5942018: 3,6482019: 3,4852020: 3,0842021: 3,0922022: 1,6382023: 1,6162024: 1,3202025: 712
2007high 4,352 (2016) · low 64 (2007)2025

MAUDE reports naming product code DSI, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20077151464
20085708156
20096733279
201061115823
201161143793
201231131766
20131—0795
2014420001,000
2015912701,645
2016622404,352
20170—03,594
20182—13,648
2019324343,485
20202—23,084
20210—03,092
20220—11,638
20232—21,616
20241—01,320
20251—18712
20261—1—

What is it indicated for?

The CIC Pro Clinical Information Center Central Station is intended to provide clinicians with adult, pediatric and neonatal patient data in a centralized location within a hospital or clinical environment. The CIC Pro Central Station is intended to collect information from a network and display this data. This data includes physiological, patient demographic and / or other non-medical information. Physiological parameters and waveforms from GE Medical…

Read the full statement (149 words)

The CIC Pro Clinical Information Center Central Station is intended to provide clinicians with adult, pediatric and neonatal patient data in a centralized location within a hospital or clinical environment.

The CIC Pro Central Station is intended to collect information from a network and display this data. This data includes physiological, patient demographic and / or other non-medical information.

Physiological parameters and waveforms from GE Medical Systems Information Technologies monitors and telemetry systems can be displayed and printed from the CIC Pro Central Station. Beat to beat patient information for all parameters and waveforms from the bedside and telemetry systems can be displayed.

The CIC Pro Central Station supports the ability to access information from GE Medical Systems Information Technologies’ products in a web browser format. Additionally, CIC Pro Central Station supports the ability to access patient information collected from the Unity network and stored on a network server

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K032370: Cic Pro Clinical Information Center Central Station.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K032370

Report an extraction error

Tell us what is wrong; we check it against the FDA summary.

Are you the manufacturer?

Send a correction or an update to this page, for example a newer model or a public statement about a recall.

Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026