510(k) Report

510(k) · Cleared

Cleared

G-Scan Brio

K133490510(k) SpecialCleared Dec 30, 201347-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

Esaote, S.p.A. · LNH System, Nuclear Magnetic Resonance Imaging

Cleared on Dec 30, 2013 as substantially equivalent to K122006 (Esaote, S.p.A., 2012) after a 47-day review. Its family tree reaches back 14 generations to 1991. 10 later devices descend from it.

Decided
Dec 30, 2013
Review
47 days
Class
Class II
Product code
LNH
Recalls
None
Predicates
1

Its longest line of descent runs back 14 generations to K911667 (1991). 48 ancestors in all. 10 later devices descend from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2006: 1 other ancestor2004: 3 other ancestors2001: 4 other ancestors2000: 4 other ancestors1994: 4 other ancestors1999: 1 other ancestor1998: 1 other ancestor1997: 2 other ancestors1996: 1 other ancestor1995: 3 other ancestors1993: 4 other ancestors1992: 2 other ancestors1991: 4 other ancestors2015: 2 descendants cleared2016: 3 descendants cleared2026: 3 descendants cleared2022: 1 descendant cleared2024: 1 descendant clearedK911667 · Hitachi MRP-7000 Magnetic Rosonance Device · Hitachi Medical Systems America, Inc. · 1991 · recalledK963262 · Artoscan M · Biosound, Inc. · 1997K981358 · Artoscan S · Biosound Esaote, Inc. · 1998K990968 · E-SCAN · Biosound Esaote, Inc. · 1999K020164 · E-Scan XQ · Biosound Esaote, Inc. · 2002K032121 · Modification to E-Scan XQ · Esaote, S.p.A. · 2003K042236 · G-SCAN · Esaote, S.p.A. · 2004×2: 2 generations cleared close together, K060956 (2006), K061429 (2006) K080968 · S-Scan, G-Scan, Dynamic Mri Software for C-Scan, E-Scanxq & E-Scan Opera · Esaote, S.p.A. · 2008K092469 · O-Scan MR System · Esaote, S.p.A. · 2009K110238 · G-SCAN · Esaote, S.p.A. · 2011K111803 · G-SCAN · Esaote, S.p.A. · 2011K122006 · G-Scan Brio · Esaote, S.p.A. · 20121990200020102020
  1. Root · 14 generations backK911667 Hitachi MRP-7000 Magnetic Rosonance DeviceHitachi Medical Systems America, Inc. · 1991 · Recalled
  2. 10 generations between
  3. 3 generations backK110238 G-SCANEsaote, S.p.A. · 2011
  4. 2 generations backK111803 G-SCANEsaote, S.p.A. · 2011
  5. 1 generation backK122006 G-Scan BrioEsaote, S.p.A. · 2012
  6. This deviceK133490 G-Scan BrioEsaote, S.p.A. · 2013
  7. Descendant · cites it directly · 9 of its ownK142421 G-scan BrioEsaote, S.p.A. · 2015 · Recalled
  8. Descendant · 2 generations on · 8 of its ownK151668 S-scanEsaote, S.p.A. · 2015
  9. Descendant · 3 generations on · 7 of its ownK153039 MRI Dynamic Analysis PlusEsaote, S.p.A. · 2016
  10. Descendant · 4 generations on · 6 of its ownK161238 S-scanEsaote, S.p.A. · 2016
  11. Descendant · 2 generations on · 5 of its ownK161973 G-scan Brio, S-scanEsaote, S.p.A. · 2016
Show all 14 generations
  1. Root · 14 generations backK911667 Hitachi MRP-7000 Magnetic Rosonance DeviceHitachi Medical Systems America, Inc. · 1991 · Recalled
  2. 13 generations backK963262 Artoscan MBiosound, Inc. · 1997
  3. 12 generations backK981358 Artoscan SBiosound Esaote, Inc. · 1998
  4. 11 generations backK990968 E-SCANBiosound Esaote, Inc. · 1999
  5. 10 generations backK020164 E-Scan XQBiosound Esaote, Inc. · 2002
  6. 9 generations backK032121 Modification to E-Scan XQEsaote, S.p.A. · 2003
  7. 8 generations backK042236 G-SCANEsaote, S.p.A. · 2004
  8. 7 generations backK060956 G-Scan-Model 9800020000, E-Scan Model 9800010000 and E-Scan…Esaote, S.p.A. · 2006
  9. 6 generations backK061429 Dynamic Mri Software Option for C-Scan, E-Scan XQ and E-Scan OperaEsaote, S.p.A. · 2006
  10. 5 generations backK080968 S-Scan, G-Scan, Dynamic Mri Software for C-Scan, E-Scanxq & E-Scan…Esaote, S.p.A. · 2008
  11. 4 generations backK092469 O-Scan MR SystemEsaote, S.p.A. · 2009
  12. 3 generations backK110238 G-SCANEsaote, S.p.A. · 2011
  13. 2 generations backK111803 G-SCANEsaote, S.p.A. · 2011
  14. 1 generation backK122006 G-Scan BrioEsaote, S.p.A. · 2012
  15. This deviceK133490 G-Scan BrioEsaote, S.p.A. · 2013

Showing 5 of 10 descendants. See all descendants

Descendants cleared per year

2015: 22016: 32022: 12024: 12026: 3
2015high 3 (2016) · low 0 (2017)2026

Most influential descendants

Showing 5 of 10 · See all
  • K142421G-scan BrioEsaote, S.p.A. · 2015 · cites it directly9descendants
  • K151668S-scanEsaote, S.p.A. · 2015 · 2 generations on8descendants
  • K153039MRI Dynamic Analysis PlusEsaote, S.p.A. · 2016 · 3 generations on7descendants
  • K161238S-scanEsaote, S.p.A. · 2016 · 4 generations on6descendants
  • K161973G-scan Brio, S-scanEsaote, S.p.A. · 2016 · 2 generations on5descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−14K911667Hitachi MRP-7000 Magnetic Rosonance DeviceHitachi Medical Systems America, Inc.19912
−13K963262Artoscan MBiosound, Inc.1997—
−12K981358Artoscan SBiosound Esaote, Inc.1998—
−11K990968E-SCANBiosound Esaote, Inc.1999—
−10K020164E-Scan XQBiosound Esaote, Inc.2002—
−9K032121Modification to E-Scan XQEsaote, S.p.A.2003—
−8K042236G-SCANEsaote, S.p.A.2004—
−7K060956G-Scan-Model 9800020000, E-Scan Model 9800010000 and E-Scan…Esaote, S.p.A.2006—
−6K061429Dynamic Mri Software Option for C-Scan, E-Scan XQ and E-Scan OperaEsaote, S.p.A.2006—
−5K080968S-Scan, G-Scan, Dynamic Mri Software for C-Scan, E-Scanxq & E-Scan OperaEsaote, S.p.A.2008—
−4K092469O-Scan MR SystemEsaote, S.p.A.2009—
−3K110238G-SCANEsaote, S.p.A.2011—
−2K111803G-SCANEsaote, S.p.A.2011—
−1K122006G-Scan BrioEsaote, S.p.A.2012—
0 (this device)K133490G-Scan BrioEsaote, S.p.A.2013—
+1K142421G-scan BrioEsaote, S.p.A.20151
+2K151668S-scanEsaote, S.p.A.2015—
+3K153039MRI Dynamic Analysis PlusEsaote, S.p.A.2016—
+4K161238S-scanEsaote, S.p.A.2016—
+2K161973G-scan Brio, S-scanEsaote, S.p.A.2016—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199140
199220
199340
199440
199530
199610
199720
199810
199910
200040
200140
200430
200610

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201520
201630
202210
202410
202630
FIG. 1 — Lineage of K133490, 1991–2026Source: 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.

Planning a device in LNH? 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? (1)

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
*K122006G-Scan Brio
Summary page 1
…Common name Class Product code Manufacturer K number C-scan System, nuclear magnetic 11 LNH ESAOTE S.PA. K122006 resonance imaging 510(k) SuImmary G-scan Brio Esante Sp.A.…
Esaote, S.p.A.2012—

What descends from it? (10)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K142421G-scan BrioEsaote, S.p.A.20159

Has anything in its family been recalled? (0 Class I)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • The line of descent spans 22 years and passes through 4 companies; a new generation was cleared every 1.4 years on median.
  • 9 of the 48 ancestors have a recall of any class.
  • Of its descendants, K142421 (Esaote, S.p.A., 2015) has gone furthest, with 9 descendants of its own.

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. 2013, this device’s year, is highlighted.

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?

G-scan Brio is a Magnetic Resonance (MR) system that produces transversal, sagittal and coronal and oblique cross-section images of the limbs, joints and spinal column. It is intended for imaging portions of the upper limb, including the hand, wrist, forearm, elbow, arm and shoulder, imaging portions of the lower limb, including the foot, ankle, calf, knee, thigh and hip, imaging the temporomandibular joint and imaging the cervical spine and the lumbar…

Read the full statement (139 words)

G-scan Brio is a Magnetic Resonance (MR) system that produces transversal, sagittal and coronal and oblique cross-section images of the limbs, joints and spinal column. It is intended for imaging portions of the upper limb, including the hand, wrist, forearm, elbow, arm and shoulder, imaging portions of the lower limb, including the foot, ankle, calf, knee, thigh and hip, imaging the temporomandibular joint and imaging the cervical spine and the lumbar spine sections as portions of the spinal column.

G-scan Brio images correspond to the spatial distribution of protons (hydrogen nuclei) that determine magnetic resonance properties and are dependent on the MR parameters, including spin-lattice relaxation time (T1), spin-spin relaxation time (T2), nuclei density, flow velocity and "chemical shift". When interpreted by a medical expert trained in the use of MR equipment, the images can provide diagnostically useful information.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K133490: G-Scan Brio.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K133490

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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