510(k) Report

510(k) · Cleared

Cleared

Model CG-WHC18-H150-AP - Wrist Hand Coil 1.5T 4 CH,

K071882510(k) TraditionalCleared Jul 18, 20079-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

Shanghai Chenguang Medical Technologies Co, Ltd. · MOS Coil, Magnetic Resonance, Specialty

Cleared on Jul 18, 2007 as substantially equivalent to K022588 (Mri Devices Corp., 2002) and 1 other predicate after a 9-day review. Its family tree reaches back 1 generation to 2002. 2 later devices descend from it.

Decided
Jul 18, 2007
Review
9 days
Class
Class II
Product code
MOS
Recalls
None
Predicates
2

Its longest line of descent runs back 1 generation to K020036 (2002). 2 ancestors in all. 2 later devices descend from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2002: 1 other ancestor2009: 1 descendant cleared2014: 1 descendant clearedK020036 · Exs-63 Small Extremity Array Coil · Mri Devices Corp. · 2002200020052010201520202025
Other ancestors, by generationDescendants, by generation 1 generation back: 1 other ancestor 1 generation forward: 1 descendant2 generations forward: 1 descendant K020036 · Exs-63 Small Extremity Array Coil · Mri Devices Corp. · 20020
  1. Root · 1 generation backK020036 Exs-63 Small Extremity Array CoilMri Devices Corp. · 2002
  2. This deviceK071882 Model CG-WHC18-H150-AP - Wrist Hand Coil 1.5T 4 CH,Shanghai Chenguang Medical Technologies Co, Ltd. · 2007
  3. Descendant · cites it directly · 1 of its ownK083578 Noras CPC Multifunctional CoilNoras Mri Products GmbH · 2009
  4. Descendant · 2 generations on · 0 of its ownK140252 16 CH Multipurpose Coil VarietyNoras Rontgen-Und Medizintechnik GmbH · 2014

Most influential descendants

Showing 2 of 2 · See all
  • K083578Noras CPC Multifunctional CoilNoras Mri Products GmbH · 2009 · cites it directly1descendant
  • K14025216 CH Multipurpose Coil VarietyNoras Rontgen-Und Medizintechnik GmbH · 2014 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−1K020036Exs-63 Small Extremity Array CoilMri Devices Corp.2002—
0 (this device)K071882Model CG-WHC18-H150-AP - Wrist Hand Coil 1.5T 4 CH,Shanghai Chenguang Medical Technologies Co, Ltd.2007—
+1K083578Noras CPC Multifunctional CoilNoras Mri Products GmbH2009—
+2K14025216 CH Multipurpose Coil VarietyNoras Rontgen-Und Medizintechnik GmbH2014—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
200210

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200910
201410
FIG. 1 — Lineage of K071882, 2002–2014Source: 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 MOS? 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 MOS device

  1. #1 K253738 3.0T Air 32CH Hnascore 15.2 · 16 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
*K022588HRW-63-Int Wrist Array Coil
Summary page 1
…y Class: II Predicate Devices (Legally Marketed Devices) The predicate devices for the Wrist Hand Coil 1.5T 4ch are the Model HRW-63-INT Wrist Array coil, submitted as K022588 and Model EXS-63 Small Extremity Array Coil, submitted as K020036. Both the predicate coils are from MRI Devices Corporation. D…
Mri Devices Corp.2002—
*K020036Exs-63 Small Extremity Array Coil
Summary page 1
…dicate devices for the Wrist Hand Coil 1.5T 4ch are the Model HRW-63-INT Wrist Array coil, submitted as K022588 and Model EXS-63 Small Extremity Array Coil, submitted as K020036. Both the predicate coils are from MRI Devices Corporation. Device Description The Wrist Hand Coil 1.5T 4ch is a 4-channel pha…
Mri Devices Corp.2002—

What descends from it? (2)

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

NumberDeviceApplicantDecidedDescendants
K083578Noras CPC Multifunctional CoilNoras Mri Products GmbH20091

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?

  • None of the 2 ancestors has a recall.
  • Of its descendants, K083578 (Noras Mri Products GmbH, 2009) has gone furthest, with 1 descendant of its own.

How does its category compare?

All MOS devices

MOS Coil, Magnetic Resonance, Specialty: FDA decisions, review times, recalls and adverse event reports over 20 years. 2007, this device’s year, is highlighted.

FDA decisions per year · MOS

3in 2025

2007: 162008: 192009: 102010: 162011: 252012: 152013: 72014: 122015: 62016: 112017: 92018: 102019: 32020: 52021: 42022: 112023: 102024: 102025: 32026 (partial year): 10
2007high 25 (2011) · low 3 (2019)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · MOS

59in 2025

2007: 19 days median2008: 33 days median2009: 43 days median2010: 78 days median2011: 57 days median2012: 49 days median2013: 87 days median2014: 60 days median2015: 58 days median2016: 42 days median2017: 63 days median2018: 30 days median2019: 178 days median2020: 51 days median2021: 41 days median2022: 79 days median2023: 59 days median2024: 39 days median2025: 59 days median2026 (partial year): 45 days median
2007high 178 (2019) · low 19 (2007)2026

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

Recalls per year · MOS

13in 2024

2008: 22010: 12012: 12015: 22019: 82020: 12024: 13
2007high 13 (2024) · low 0 (2007)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · MOS

2in 2025

2007: 42008: 22009: 52010: 132011: 72012: 122013: 102014: 42015: 52016: 72017: 92018: 72019: 82020: 22021: 32022: 52023: 42024: 82025: 2
2007high 13 (2010) · low 2 (2008)2025

MAUDE reports naming product code MOS, 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
2007161904
2008193322
2009104305
20101678113
2011255707
20121549112
2013787010
2014126004
201565825
2016114207
201796309
2018103007
2019317888
202055112
202144103
2022117905
2023105904
20241039138
202535902
202610450—

What is it indicated for?

The coil is intended to be used in conjunction with a PHILIPS 1.5T MRI scanner as an accessory to produce images of the wrist, hand and elbow.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K071882: Model CG-WHC18-H150-AP - Wrist Hand Coil 1.5T 4 CH,.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K071882

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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