# K050489: Innova 2100

- Pathway: 510(k) (Traditional)
- Applicant: Ge Medical Systems, LLC
- Decided: Mar 11, 2005 after 14 days
- Product code: OWB (Interventional Fluoroscopic X-Ray System)
- Device class: 2
- Regulation: 21 CFR 892.1650
- Recalls of this device: 27 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 4 generations back to K890348 (1989). 8 ancestors in all.
75 later devices descend from it; 5 cite it directly.
0 of 84 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K031637: Innova 3100, GE Medical Systems (2003) Summary page 1.
- K022322: Innova and Innova 2000 S, Ge Medical Systems, Inc. (2002) Summary page 1.
- K993037: LCV+ Version 2, Ge Medical Systems, Inc. (2000) Summary page 1.

## Most influential descendants
- K052412: Innova 2100-IQ, Innova 3100, Innova 3100-IQ, Innova 4100, and Innova 4100-IQ (2005), 74 descendants of its own
- K060259: Digital Fluoroscopic Imaging Systems - Innova  3131 & Innova 2121 (2006), 47 descendants of its own
- K081582: Infx-8000V, Infinix-Cfi and Infinix Vfi (2008), 23 descendants of its own
- K061163: Innova 2121IQ, Innova 3131IQ, Innova 4100, Innova 4100IQ, Innova 3100, Innova 3100IQ, Innova 2100IQ with Innova Ivus Opt (2006), 22 descendants of its own
- K101868: Infinix-I Interventional Angiography System Model Infx-8000V (2010), 21 descendants of its own

## Recalls of this device
- Dec 11, 2013 · Class II · Z-1163-2014: GE Healthcare has become aware of a potential safety issue involving the innova systems. The Innova system can unexpectedly stop delivering X-rays after a power-on or a reset cycle which may result in
- Jan 21, 2013 · Class II · Z-0947-2013: A locking nut might loosen out of the overhead Video Monitor Suspension yoke affecting Advantx, Innova 2000, Innova 2100IQ, Innova 3100, Innova 3100IQ, Innova 4100, and Innova 4100IQ Cardiovascular X-
- Dec 20, 2011 · Class II · Z-1318-2013: While performing a fluoroscopic examination on the GE Innova systems, there is a potential of nonrecoverable loss of imaging modes with no advance warning, due to a relay failure in the power distribu
- Oct 21, 2011 · Class II · Z-1142-2013: As part of GE Innova IQ table introduction, a label was designed to be affixed on the front Cover of the Gantry Pivot section. This safety label is missing on systems manufactured between March 2010 a
- Feb 4, 2011 · Class II · Z-0934-2013: Exposed high voltage wires inside the cabinet . On a cable located in the system cabinet, two of the shrink tubings covering the 400V live cable leave an area potentially unprotected.
- Jun 3, 2010 · Not classified · Z-1922-2010: GE Healthcare has become aware of a potential loss of gantry and table motions affecting Innova 2100IQ, 3100, 3100IQ, 4100 and 4100IQ systems with InnovaIQ Table that may impact patient safety.
- Jun 3, 2010 · Not classified · Z-1923-2010: GE Healthcare has become aware of a potential loss of gantry and table motions affecting Innova 2100IQ, 3100, 3100IQ, 4100 and 4100IQ systems with InnovaIQ Table that may impact patient safety.
- Jun 3, 2010 · Not classified · Z-1921-2010: GE Healthcare has become aware of a potential loss of gantry and table motions affecting Innova 2100IQ, 3100, 3100IQ, 4100 and 4100IQ systems with InnovaIQ Table that may impact patient safety.
- Mar 24, 2010 · Not classified · Z-1661-2010: A potential software failure related to the Worklist functionality has been identified on a subset of Innova 2100IQ, 3100IQ and 4100IQ systems. When using the Worklist function to import patient data 
- Dec 22, 2009 · Not classified · Z-0617-2010: Potential table rotation of Omega IV and Omega V tables affecting Advantx-E and Innova 2000, 2100IQ, 3100, 3100IQ, 4100, 4100IQ, 2121IQ and 3131IQ cardiovascular X-ray imaging systems. Due to potentia
- Aug 5, 2009 · Not classified · Z-0408-2011: GE Healthcare has become aware of a potential issue regarding Innova systems with GE Fluoro UPS 20KVA that may impact patient safety. GE Fluoro UPS 20KVA (Uninterrupted Power Supply) is used to mainta
- Apr 16, 2009 · Not classified · Z-0136-2010: Potential pump failure associated with the Coolix 4000 chiller of the Innova single plane and biplane systems that may stop the chiller from working. If a chiller failure occurs, the user will be info
- Jul 25, 2008 · Not classified · Z-2436-2008: The charger and / or battery of the PDB may fail earlier than expected with no advance warning and thus cause the system to shut down.
- Jun 24, 2008 · Not classified · Z-2361-2008: GE Healthcare has become aware of 2 potential conditions that could occur with the MAVIG GD Monitor Suspension that is used with Advantx-E, Innova 2000, 21000IQ, 3100/3100IQ, 4100/4100IQ and 2121 IQ/3
- Jun 17, 2008 · Not classified · Z-1474-2009: GE Healthcare has become aware that a few customers have experienced an unusual occurrence of system lockups on Innova single plane cardiovascular X-ray imaging systems while using the image auto-arch
- Jan 30, 2008 · Not classified · Z-0473-2009: Software error, computer: GE Healthcare has became aware of an issue with Error Management affecting the Innova 2100, 3100/3100 IQ & 4100/4100IQ. It was reported that when the foot switch was pressed,
- Jan 14, 2008 · Not classified · Z-2039-2008: Risk of sudden table drop on Omega IV and Omega V tables on GE Healthcare Advantx-E as well as on Innova 2000, 2100IQ, 3100/3100 IQ and 4100/4100IQ cardiovascular X-ray system
- Nov 15, 2007 · Not classified · Z-0690-2008: Frozen Image Problems: During an acquisition (fluoro and/or record), there have been cases reported where an image became "frozen" on the DL (digital leader acquisition system) live monitor screen. In
- Mar 26, 2007 · Not classified · Z-0871-2007: Measurement errors during the computation of vessel diameters while using the Stenosis Analysis software (also known as Quantitative Coronary Analysis function-QCA) using the auto-calibration function
- Mar 26, 2007 · Not classified · Z-0870-2007: Measurement errors during the computation of vessel diameters while using the Stenosis Analysis software (also known as Quantitative Coronary Analysis function-QCA) using the auto-calibration function
- Mar 26, 2007 · Not classified · Z-0869-2007: Measurement errors during the computation of vessel diameters while using the Stenosis Analysis software (also known as Quantitative Coronary Analysis function-QCA) using the auto-calibration function
- Mar 26, 2007 · Not classified · Z-1044-2007: Caution on the non-detection of small invasive objects/devices, which project out from the skin surfaces (e.g. biopsy or other needles) while using the Innova Sense software option designed for patien
- Mar 26, 2007 · Not classified · Z-1043-2007: Caution on the non-detection of small invasive objects/devices, which project out from the skin surfaces (e.g. biopsy or other needles) while using the Innova Sense software option designed for patien
- Aug 17, 2006 · Not classified · Z-1519-2008: User was unable to hear the Innova 2100-IQ 5-minute fluoroscopy warning signal from the Table Control TSSC interface. Inability of the user to hear the audible signal indicating the completion of any 
- Aug 17, 2006 · Not classified · Z-1520-2008: User was unable to hear the Innova 2100-IQ 5-minute fluoroscopy warning signal from the Table Control TSSC interface. Inability of the user to hear the audible signal indicating the completion of any 
- Aug 17, 2006 · Not classified · Z-1518-2008: User was unable to hear the Innova 2100-IQ 5-minute fluoroscopy warning signal from the Table Control TSSC interface. Inability of the user to hear the audible signal indicating the completion of any 
- Jun 6, 2006 · Not classified · Z-1088-2007: The systems do not contain a certification label on the C2 Cabinet (Beam-limiting control).

## Indications for use
The Innova 2100-1Q system is indicated for use in generating fluoroscopic images of human anatomy for vascular angiography diagnostic and interventional procedures, and optionally, rotational angiography procedures. It is also indicated for generating fluoroscopic images of human anatomy for cardiology diagnostic and interventional procedures. It is intended to replace fluoroscopic images obtained through image intensifier technology. This device is not intended for mammography applications.

Source page: https://510kreport.com/device/K050489
Methodology: https://510kreport.com/methodology