# K041111: Magnetom C! MR System

- Pathway: 510(k) (Traditional)
- Applicant: Siemens Medical Solutions USA, Inc.
- Decided: Jul 16, 2004 after 79 days
- Product code: LNH (System, Nuclear Magnetic Resonance Imaging)
- Device class: 2
- Regulation: 21 CFR 892.1000
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K970852 (1997). 2 ancestors in all.
38 later devices descend from it; 1 cites it directly.
0 of 41 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K003192: Magnetic Concerto, Siemens Medical Solutions USA, Inc. (2000) Summary page 2.
- K970852: Magnetom Project 024 System (Numaris 3.5 Software), Siemens Medical Solutions USA, Inc. (1997) Summary page 2.

## Most influential descendants
- K043030: Magnetom C! MR System (2004), 37 descendants of its own
- K063207: S-Scan Mri System (2006), 34 descendants of its own
- K080968: S-Scan, G-Scan, Dynamic Mri Software for C-Scan, E-Scanxq & E-Scan Opera (2008), 24 descendants of its own
- K092469: O-Scan MR System (2009), 18 descendants of its own
- K110238: G-SCAN (2011), 15 descendants of its own

## Indications for use
The MAGNETOM C! is indicated for use as magnetic resonance diagnostic devices (MRDD) that produce transverse, sagittal, coronal and oblique cross sectional images, spectroscopic images and/or spectra, and that display the internal structure and/or function of the head, body, or extremities. These images and/or spectra when interpreted by a trained physician yield information that may assist in diagnosis. The MAGNETOM C! may also be used for imaging during interventional procedures when performed with MR compatible devices such as, in room display and MR safe biopsy needles

Source page: https://510kreport.com/device/K041111
Methodology: https://510kreport.com/methodology