SOFTWARE VERSION, D1.3 AND A1.3 FOR MAGNETOM

K893640 · Siemens Medical Solutions USA, Inc. · LNH · Aug 2, 1989 · Radiology

Device Facts

Record IDK893640
Device NameSOFTWARE VERSION, D1.3 AND A1.3 FOR MAGNETOM
ApplicantSiemens Medical Solutions USA, Inc.
Product CodeLNH · Radiology
Decision DateAug 2, 1989
DecisionSESE
Submission TypeTraditional
Regulation21 CFR 892.1000
Device ClassClass 2

Regulatory Classification

Identification

A magnetic resonance diagnostic device is intended for general diagnostic use to present images which reflect the spatial distribution and/or magnetic resonance spectra which reflect frequency and distribution of nuclei exhibiting nuclear magnetic resonance. Other physical parameters derived from the images and/or spectra may also be produced. The device includes hydrogen-1 (proton) imaging, sodium-23 imaging, hydrogen-1 spectroscopy, phosphorus-31 spectroscopy, and chemical shift imaging (preserving simultaneous frequency and spatial information).

Special Controls

*Classification.* Class II (special controls). A magnetic resonance imaging disposable kit intended for use with a magnetic resonance diagnostic device only is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to the limitations in § 892.9.

Innolitics

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