# Discovery IQ

> Active: United States. Medical device record on deviCERTS, compiled from public registries.

- Canonical page: <https://devicerts.com/devices/discovery-iq>
- Manufacturer: [GE Medical Systems, L.L.C.](https://devicerts.com/manufacturers/ge-medical-systems-l-l-c) (FDA registration: United States)
- Device class: Class II (US FDA)
- FDA product code: JAK, KPS
- GMDN: Full-body CT system (37618)

## Registrations and authorizations

- **GUDID** · GUDID listing · United States · UDI-DI 00840682103107 · listed 2016-08-01 · status: Listed (GUDID: in commercial distribution)
- **GUDID** · FDA 510(k) · United States · K141477 · issued 2014-09-18 · status: Active · from GUDID

## Recalls

- Z-1748-2019 · Class II · ongoing · initiated 2019-02-12: GE Healthcare PET/CT Table Stop Without Stopping X-Ray Exposure
- Z-2578-2018 · Class II · terminated · initiated 2018-05-24: Some CT and CT/PET systems recently installed with a GE supplied A! electrical panel may not be properly wired to the partial system UPS (Uninteruptible Power Supply).
- Z-2192-2017 · Class II · terminated · initiated 2017-05-19: It was discovered that an issue has been identified that can result in a scan starting before the prescribed delay has completed.

## Identity

- Trade name: Discovery [FDA GUDID (AccessGUDID)]
- Generic name: Full-body CT system [FDA GUDID (AccessGUDID)]
- Model / reference: IQ [FDA GUDID (AccessGUDID)]

## Identifiers

- Primary DI / UDI-DI: 00840682103107 [FDA GUDID (AccessGUDID)]
- 510(k) Number: K141477 [FDA GUDID (AccessGUDID)]
- FDA product code: JAK [FDA GUDID (AccessGUDID)]; KPS [FDA GUDID (AccessGUDID)]
- GMDN term: Full-body CT system (37618) [FDA GUDID (AccessGUDID)]

## Classification

- Device class: Class II [FDA GUDID (AccessGUDID)]
- Regulation number: 892.1750 [FDA GUDID (AccessGUDID)]; 892.1200 [FDA GUDID (AccessGUDID)]
- GUDID distribution status: In Commercial Distribution [FDA GUDID (AccessGUDID)]

## Properties

- Prescription use: Yes [FDA GUDID (AccessGUDID)]
- Serial number: Yes [FDA GUDID (AccessGUDID)]
- Manufacturing date: Yes [FDA GUDID (AccessGUDID)]
- Supplied sterile: No [FDA GUDID (AccessGUDID)]
- Sterilise before use: No [FDA GUDID (AccessGUDID)]
- Single use: No [FDA GUDID (AccessGUDID)]
- Implantable: No [FDA GUDID (AccessGUDID)]
- Contains latex: No [FDA GUDID (AccessGUDID)]
- Over-the-counter: No [FDA GUDID (AccessGUDID)]
- Convenience kit: No [FDA GUDID (AccessGUDID)]
- Combination product: No [FDA GUDID (AccessGUDID)]
- HCT/P: No [FDA GUDID (AccessGUDID)]
- Premarket exempt: No [FDA GUDID (AccessGUDID)]
- Lot / batch number: No [FDA GUDID (AccessGUDID)]
- Expiration date: No [FDA GUDID (AccessGUDID)]

## Source and citation

- Cite as: Discovery IQ, GE Medical Systems, L.L.C. deviCERTS medical device catalogue. https://devicerts.com/devices/discovery-iq (data as of 2026-11-14).
- Data sources: [FDA GUDID (AccessGUDID)](https://accessgudid.nlm.nih.gov/), [FDA recalls](https://open.fda.gov/apis/device/recall/)
- Registry records last synced: 2026-10-23
- Statuses computed as of: 2026-11-14
- JSON: <https://devicerts.com/devices/discovery-iq.json>
- Licence: [CC BY 4.0](https://creativecommons.org/licenses/by/4.0/). The deviCERTS layout and text are licensed under CC BY 4.0. Registry data remain under their source terms: U.S. FDA data (openFDA, AccessGUDID) are U.S. public domain; EUDAMED data are subject to the European Commission reuse terms.
- Attribution: DevicErts, https://devicerts.com/devices/discovery-iq
- Compiled by deviCERTS (devicerts.com) from public medical device registries (EUDAMED, European Commission; U.S. FDA via openFDA; AccessGUDID, U.S. National Library of Medicine). deviCERTS is not an official register and gives no regulatory advice: the record in the registry itself prevails.