510(k) Report

510(k) · Cleared

Cleared

Magnetom Symphony a Tim System

K050199510(k) TraditionalCleared Feb 18, 200521-day reviewClass II21 CFR 892.1000

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

Siemens Medical Solution · LNH System, Nuclear Magnetic Resonance Imaging

Cleared on Feb 18, 2005 as substantially equivalent to K032428 (Siemens Medical Solutions USA, Inc., 2003) and 1 other predicate after a 21-day review. Its family tree reaches back 2 generations to 1997. 22 of the 426 devices in its family, counting itself, have a Class I recall. 422 later devices descend from it.

Decided
Feb 18, 2005
Review
21 days
Class
Class II
Product code
LNH
Recalls
None
Predicates
2

Its longest line of descent runs back 2 generations to K971684 (1997). 3 ancestors in all. 422 later devices descend from it, 3 citing it directly. 22 of the 426 devices in this family, counting this one, have a Class I recall.

Other ancestors, by year clearedDescendants, by year cleared 1999: 1 other ancestor2006: 4 descendants cleared2005: 1 descendant cleared2008: 7 descendants cleared2024: 31 descendants cleared2023: 41 descendants cleared, 3 with a Class I recall32015: 18 descendants cleared, 1 with a Class I recall12012: 13 descendants cleared, 2 with a Class I recall22007: 2 descendants cleared, 1 with a Class I recall12013: 23 descendants cleared, 2 with a Class I recall22009: 4 descendants cleared2011: 12 descendants cleared2010: 5 descendants cleared, 1 with a Class I recall12018: 26 descendants cleared, 2 with a Class I recall22014: 15 descendants cleared2020: 39 descendants cleared, 3 with a Class I recall32019: 29 descendants cleared, 1 with a Class I recall12016: 15 descendants cleared, 1 with a Class I recall12017: 23 descendants cleared, 1 with a Class I recall12025: 32 descendants cleared, 1 with a Class I recall12021: 18 descendants cleared, 1 with a Class I recall12022: 37 descendants cleared, 2 with a Class I recall22026: 27 descendants clearedK971684 · Magnetom Project 047 System (Numaris 3.5 Software) · Siemens Medical Solutions USA, Inc. · 1997 · recalledK032428 · Magnetom Avanto MR System · Siemens Medical Solutions USA, Inc. · 2003 · recalled1995200020052010201520202025
Other ancestors, by generationDescendants, by generation 2 generations back: 1 other ancestor 1 generation forward: 3 descendants2 generations forward: 10 descendants, 1 with a Class I recall13 generations forward: 23 descendants, 4 with a Class I recall44 generations forward: 37 descendants, 2 with a Class I recall25 generations forward: 62 descendants, 3 with a Class I recall36 generations forward: 65 descendants, 2 with a Class I recall27 generations forward: 61 descendants, 1 with a Class I recall18 generations forward: 39 descendants, 1 with a Class I recall19 generations forward: 42 descendants, 1 with a Class I recall110 generations forward: 29 descendants, 3 with a Class I recall311 generations forward: 19 descendants, 1 with a Class I recall112 generations forward: 9 descendants, 3 with a Class I recall313 generations forward: 9 descendants14 generations forward: 9 descendants15 generations forward: 3 descendants16 generations forward: 1 descendant17 generations forward: 1 descendant K032428 · Magnetom Avanto MR System · Siemens Medical Solutions USA, Inc. · 2003 · recalledK971684 · Magnetom Project 047 System (Numaris 3.5 Software) · Siemens Medical Solutions USA, Inc. · 1997 · recalled0+5+10+15
  1. Root · 2 generations backK971684 Magnetom Project 047 System (Numaris 3.5 Software)Siemens Medical Solutions USA, Inc. · 1997 · Recalled
  2. 1 generation backK032428 Magnetom Avanto MR SystemSiemens Medical Solutions USA, Inc. · 2003 · Recalled
  3. This deviceK050199 Magnetom Symphony a Tim SystemSiemens Medical Solution · 2005
  4. Descendant · cites it directly · 312 of its ownK052164 Magnetom Systems with Software Syngo MR 2006ASiemens Medical Solutions USA, Inc. · 2005
  5. Descendant · cites it directly · 308 of its ownK062454 Magnetom Systems - I-Class and T-Class ReleasesSiemens Medi Cal Solutions, Inc. · 2006
  6. Descendant · 2 generations on · 300 of its ownK072237 Magnetom VerioSiemens Medical Solutions USA, Inc. · 2007 · Recalled (Class I)
  7. Descendant · 2 generations on · 229 of its ownK082427 Syngo MR B17Siemens Medical Solutions USA, Inc. · 2008
  8. Descendant · 2 generations on · 228 of its ownK071925 Magnetom EssenzaSiemens Medical Solutions USA, Inc. · 2007 · Recalled

Showing 5 of 422 descendants. See all descendants

Descendants cleared per year

2005: 12006: 42007: 22008: 72009: 42010: 52011: 122012: 132013: 232014: 152015: 182016: 152017: 232018: 262019: 292020: 392021: 182022: 372023: 412024: 312025: 322026: 27
2005high 41 (2023) · low 1 (2005)2026

Class I recalls in this family

Most influential descendants

Showing 5 of 422 · See all
  • K052164Magnetom Systems with Software Syngo MR 2006ASiemens Medical Solutions USA, Inc. · 2005 · cites it directly312descendants
  • K062454Magnetom Systems - I-Class and T-Class ReleasesSiemens Medi Cal Solutions, Inc. · 2006 · cites it directly308descendants
  • K072237Magnetom VerioSiemens Medical Solutions USA, Inc. · 2007 · 2 generations on300descendants
  • K082427Syngo MR B17Siemens Medical Solutions USA, Inc. · 2008 · 2 generations on229descendants
  • K071925Magnetom EssenzaSiemens Medical Solutions USA, Inc. · 2007 · 2 generations on228descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−2K971684Magnetom Project 047 System (Numaris 3.5 Software)Siemens Medical Solutions USA, Inc.19974
−1K032428Magnetom Avanto MR SystemSiemens Medical Solutions USA, Inc.20034
0 (this device)K050199Magnetom Symphony a Tim SystemSiemens Medical Solution2005—
+1K052164Magnetom Systems with Software Syngo MR 2006ASiemens Medical Solutions USA, Inc.2005—
+1K062454Magnetom Systems - I-Class and T-Class ReleasesSiemens Medi Cal Solutions, Inc.2006—
+2K072237Magnetom VerioSiemens Medical Solutions USA, Inc.2007Class I
+2K082427Syngo MR B17Siemens Medical Solutions USA, Inc.2008—
+2K071925Magnetom EssenzaSiemens Medical Solutions USA, Inc.20071

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199910

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200510
200640
200721
200870
200940
201051
2011120
2012132
2013232
2014150
2015181
2016151
2017231
2018262
2019291
2020393
2021181
2022372
2023413
2024310
2025321
2026270
FIG. 1 — Lineage of K050199, 1997–2026Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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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.

22 devices in this family have a Class I recall. 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 LNH device

  1. #1 K213693 MAGNETOM Vida with syngo MR XA50Ascore 23.0 · 18 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? (2)

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
*K032428Magnetom Avanto MR System
Summary page 2
…FDA Clearance FDA ClearanceDate Number Siemens MAGNETOM 1.5 T Avanto K032428 10/16/03 Siemens MAGNETOM 1.5 T Symphony K971684 08/05/97 General Safety…
Siemens Medical Solutions USA, Inc.20034
*K971684Magnetom Project 047 System (Numaris 3.5 Software)
Summary page 2
…Number Siemens MAGNETOM 1.5 T Avanto K032428 10/16/03 Siemens MAGNETOM 1.5 T Symphony K971684 08/05/97 General Safety and Effectiveness Concerns: Operation of the MAGNETOM Symphony a Tim System is substant…
Siemens Medical Solutions USA, Inc.19974

Also cleared against K032428: 10 other devices →

What descends from it? (422)

See all 422

3 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K052164Magnetom Systems with Software Syngo MR 2006ASiemens Medical Solutions USA, Inc.2005312
K062454Magnetom Systems - I-Class and T-Class ReleasesSiemens Medi Cal Solutions, Inc.2006308
K052423Magnetom Systems with Syngo Expert - I OptionSiemens Medi Cal Solutions, Inc.2006199

Has anything in its family been recalled? (22 Class I)

No FDA recall names this device.

Relatives with a Class I recall

Class I is FDA’s most serious recall class. A recall in the family tree is context for this device, not evidence about it.

  • K072237Magnetom VerioSiemens Medical Solutions USA, Inc. · 2007 · 2 generations on · ◆ in the 2007 descendants bar of FIG. 11 Class I recall
  • K101347Magnetom Aera; Magnetom SkyraSiemens Medical Solutions USA, Inc. · 2010 · 3 generations on · ◆ in the 2010 descendants bar of FIG. 12 Class I recalls
  • K130885Magnetom Avanto-Fit, Magnetom Skyra-FitSiemens Medical Solutions USA, Inc. · 2013 · 3 generations on · ◆ in the 2013 descendants bar of FIG. 11 Class I recall
  • K121160Magnetom SpectraSiemens Medical Solutions USA, Inc. · 2012 · 3 generations on · ◆ in the 2012 descendants bar of FIG. 11 Class I recall
  • K121434Software Syngo MR D13A for the Magnetom Systems Aera/Skyra/Avanto/VerioSiemens Medi Cal Solutions, Inc. · 2012 · 3 generations on · ◆ in the 2012 descendants bar of FIG. 12 Class I recalls
  • K181613MAGNETOM Avanto, MAGNETOM Verio with software syngo MR E11DSiemens Medical Solutions USA, Inc. · 2018 · 4 generations on · ◆ in the 2018 descendants bar of FIG. 12 Class I recalls
  • K132119Magnetom Prisma, Magnetom Prisma FitSiemens Medical Solutions USA, Inc. · 2013 · 4 generations on · ◆ in the 2013 descendants bar of FIG. 11 Class I recall
  • K153343MAGNETOM Aera, MAGNETOM Skyra, MAGNETOM Prisma, MAGNETOM Prisma fitSiemens Medi Cal Solutions, Inc. · 2016 · 5 generations on · ◆ in the 2016 descendants bar of FIG. 11 Class I recall
  • K151579MAGNETOM Aera (24-channel), MAGNETOM Avanto fit, MAGNETOM Skyra fit, MAGNETOM Prisma, MAGNETOM Prisma fitSiemens Medical Solutions USA, Inc. · 2015 · 5 generations on · ◆ in the 2015 descendants bar of FIG. 12 Class I recalls
  • K200213Biograph mMR with syngo MR E11P-AP01 system softwareSiemens Medical Solutions USA, Inc. · 2020 · 5 generations on · ◆ in the 2020 descendants bar of FIG. 11 Class I recall
  • K170396MAGNETOM VidaSiemens Medical Solutions USA, Inc. · 2017 · 6 generations on · ◆ in the 2017 descendants bar of FIG. 11 Class I recall
  • K173592MAGNETOM Aera, MAGNETOM Skyra/Skyrafit, MAGNETOM Prisma/Prismafit, MAGNETOM AvantofitSiemens Medical Solutions USA, Inc. · 2018 · 6 generations on · ◆ in the 2018 descendants bar of FIG. 12 Class I recalls

Nearest 12 of 22 shown.

What does this lineage say?

  • The line of descent spans 8 years and passes through 2 companies; a new generation was cleared every 6.2 years on median.
  • 3 of the 3 ancestors have a recall of any class.
  • Of its descendants, K052164 (Siemens Medical Solutions USA, Inc., 2005) has gone furthest, with 312 descendants of its own.
  • 10 other devices also cite its predicate K032428.

How does its category compare?

All LNH devices

LNH System, Nuclear Magnetic Resonance Imaging: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · LNH

26in 2025

2007: 122008: 192009: 172010: 122011: 162012: 222013: 192014: 172015: 192016: 202017: 182018: 292019: 262020: 322021: 272022: 302023: 302024: 262025: 262026 (partial year): 24
2007high 32 (2020) · low 12 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · LNH

122in 2025

2007: 35 days median2008: 53 days median2009: 70 days median2010: 94 days median2011: 81 days median2012: 89 days median2013: 108 days median2014: 108 days median2015: 140 days median2016: 108 days median2017: 98 days median2018: 128 days median2019: 62 days median2020: 121 days median2021: 87 days median2022: 74 days median2023: 124 days median2024: 104 days median2025: 122 days median2026 (partial year): 126 days median
2007high 140 (2015) · low 35 (2007)2026

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

Recalls per year · LNH

8in 2025

2007: 252008: 122009: 72010: 172011: 112012: 52013: 22014: 132015: 12, 2 Class I2016: 12018: 712019: 52020: 42021: 412022: 132023: 10, 1 Class I2024: 42025: 8, 5 Class I2026 (partial year): 43
2007high 71 (2018) · low 0 (2017)2026

Class I (8 since 2007) Class II/III not classified

Adverse event reports per year · LNH

1,263in 2025

2007: 1142008: 1672009: 1942010: 1652011: 1822012: 1702013: 1072014: 1192015: 1132016: 1352017: 1212018: 1582019: 1582020: 982021: 842022: 1382023: 1592024: 2812025: 1,263
2007high 1,263 (2025) · low 84 (2021)2025

MAUDE reports naming product code LNH, 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
2007123525114
2008195312167
200917707194
2010129417165
2011168111182
201222895170
2013191082107
20141710813119
20151914012 (2)113
2016201081135
201718980121
20182912871158
201926625158
202032121498
202127874184
2022307413138
20233012410 (1)159
2024261044281
2025261228 (5)1,263
20262412643—

What is it indicated for?

The "MAGNETOM Symphony a Tim System" is indicated for use as a magnetic resonance diagnostic device (MRDD) that produces transverse, sagittal, coronal and oblique cross sectional images, spectroscopic images and/or spectra, and that displays 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 Symphony a Tim System" may also be used for imaging during interventional procedures performed with MR compatible devices such as, in room display and MR safe biopsy needles.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K050199: Magnetom Symphony a Tim System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K050199

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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