510(k) Report

510(k) · Cleared

Cleared

GUS610 Blood pressure monitor

K222160510(k) TraditionalCleared Nov 22, 2022125-day reviewClass II21 CFR 870.1130

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

Globalcare Medical Technology Co., Ltd. · DXN System, Measurement, Blood-Pressure, Non-Invasive

Cleared on Nov 22, 2022 as substantially equivalent to K192609 (Globalcare Medical Technology Co., Ltd., 2020) after a 125-day review. Its family tree reaches back 10 generations to 2000. 1 later device descends from it.

Decided
Nov 22, 2022
Review
125 days
Class
Class II
Product code
DXN
Recalls
None
Predicates
1

Its longest line of descent runs back 10 generations to K001670 (2000). 1 later device descends from it, 1 citing it directly.

  1. Root · 10 generations backK001670 Automatic Blood Pressure Monitor with Intellisense, Model Hem-757Omron Healthcare, Inc. · 2000
  2. 6 generations between
  3. 3 generations backK120672 KD-936 Fully Automatic Wireless Blood Pressure MonitorAndon Health Co, Ltd. · 2012
  4. 2 generations backK141984 Fully Automatic Electronic Blood Pressure MonitorAndon Health Co, Ltd. · 2015
  5. 1 generation backK192609 Globalcare Blood Pressure MonitorGlobalcare Medical Technology Co., Ltd. · 2020
  6. This deviceK222160 GUS610 Blood pressure monitorGlobalcare Medical Technology Co., Ltd. · 2022
  7. Descendant · cites it directly · 0 of its ownK250136 Globalcare Blood Pressure Monitor (GUS610)Globalcare Medical Technology Co., Ltd. · 2025
Show all 10 generations
  1. Root · 10 generations backK001670 Automatic Blood Pressure Monitor with Intellisense, Model Hem-757Omron Healthcare, Inc. · 2000
  2. 9 generations backK030358 KD-622 Fully Automatic Electronic Blood Pressure MonitorKodon (Tianjin)Electronic&Electrical Apparatus Co., · 2003
  3. 8 generations backK070828 KD-595 Fully Automatic Electronic Blood Pressure MonitorKodon (Tianjin)Electronic&Electrical Apparatus Co., · 2007
  4. 7 generations backK080319 KD-591 Fully Automatic Electronic Blood Pressure MonitorAndon Health Co, Ltd. · 2008
  5. 6 generations backK090963 Fully Automatic Electronic Blood Pressure Monitor, Model KD-556Andon Health Co, Ltd. · 2009
  6. 5 generations backK101950 Fully Automatic Electronic Blood Pressure Monitor Model KD-930Andon Health Co, Ltd. · 2010
  7. 4 generations backK102939 Fully Automatic Electronic Blood Pressure Monitor Model KD-931Andon Health Co, Ltd. · 2011
  8. 3 generations backK120672 KD-936 Fully Automatic Wireless Blood Pressure MonitorAndon Health Co, Ltd. · 2012
  9. 2 generations backK141984 Fully Automatic Electronic Blood Pressure MonitorAndon Health Co, Ltd. · 2015
  10. 1 generation backK192609 Globalcare Blood Pressure MonitorGlobalcare Medical Technology Co., Ltd. · 2020
  11. This deviceK222160 GUS610 Blood pressure monitorGlobalcare Medical Technology Co., Ltd. · 2022

Most influential descendants

Showing 1 of 1 · See all
  • K250136Globalcare Blood Pressure Monitor (GUS610)Globalcare Medical Technology Co., Ltd. · 2025 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−10K001670Automatic Blood Pressure Monitor with Intellisense, Model Hem-757Omron Healthcare, Inc.2000—
−9K030358KD-622 Fully Automatic Electronic Blood Pressure MonitorKodon (Tianjin)Electronic&Electrical Apparatus Co.,2003—
−8K070828KD-595 Fully Automatic Electronic Blood Pressure MonitorKodon (Tianjin)Electronic&Electrical Apparatus Co.,2007—
−7K080319KD-591 Fully Automatic Electronic Blood Pressure MonitorAndon Health Co, Ltd.2008—
−6K090963Fully Automatic Electronic Blood Pressure Monitor, Model KD-556Andon Health Co, Ltd.2009—
−5K101950Fully Automatic Electronic Blood Pressure Monitor Model KD-930Andon Health Co, Ltd.2010—
−4K102939Fully Automatic Electronic Blood Pressure Monitor Model KD-931Andon Health Co, Ltd.2011—
−3K120672KD-936 Fully Automatic Wireless Blood Pressure MonitorAndon Health Co, Ltd.2012—
−2K141984Fully Automatic Electronic Blood Pressure MonitorAndon Health Co, Ltd.2015—
−1K192609Globalcare Blood Pressure MonitorGlobalcare Medical Technology Co., Ltd.2020—
0 (this device)K222160GUS610 Blood pressure monitorGlobalcare Medical Technology Co., Ltd.2022—
+1K250136Globalcare Blood Pressure Monitor (GUS610)Globalcare Medical Technology Co., Ltd.2025—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202510
FIG. 1 — Lineage of K222160, 2000–2025Source: 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 DXN? 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 DXN device

  1. #1 K222125 Arm Blood Pressure Monitor, models AOJ-30A…score 18.5 · 8 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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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
*K192609Globalcare Blood Pressure Monitor
Summary page 7
…he GUS610 Blood Pressure Monitor is: Predicate Device: Blood Pressure Monitor Model GUS622 Sponsor: Globalcare, China 510(k) Number: K192609 Clearance Date: 21 April 2020 FDA Product Code: DXN Classification Name: Noninvasive blood pressure measur…
Globalcare Medical Technology Co., Ltd.2020—

Also cleared against K192609: 1 other device →

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K250136Globalcare Blood Pressure Monitor (GUS610)Globalcare Medical Technology Co., Ltd.20250

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 2.6 years on median.
  • None of the 10 ancestors has a recall.
  • Of its descendants, K250136 (Globalcare Medical Technology Co., Ltd., 2025) has gone furthest, with 0 descendants of its own.
  • 1 other device also cites its predicate K192609.

How does its category compare?

All DXN devices

DXN System, Measurement, Blood-Pressure, Non-Invasive: FDA decisions, review times, recalls and adverse event reports over 20 years. 2022, this device’s year, is highlighted.

FDA decisions per year · DXN

28in 2025

2007: 272008: 232009: 462010: 432011: 342012: 362013: 342014: 292015: 302016: 302017: 332018: 222019: 332020: 242021: 232022: 252023: 352024: 172025: 282026 (partial year): 29
2007high 46 (2009) · low 17 (2024)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · DXN

142in 2025

2007: 118 days median2008: 82 days median2009: 73 days median2010: 94 days median2011: 72 days median2012: 116 days median2013: 150 days median2014: 133 days median2015: 97 days median2016: 144 days median2017: 184 days median2018: 235 days median2019: 156 days median2020: 198 days median2021: 190 days median2022: 137 days median2023: 182 days median2024: 107 days median2025: 142 days median2026 (partial year): 147 days median
2007high 235 (2018) · low 72 (2011)2026

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

Recalls per year · DXN

3in 2024

2008: 12009: 32011: 12013: 12016: 12019: 12024: 3
2007high 3 (2009) · low 0 (2007)2026

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

Adverse event reports per year · DXN

239in 2025

2007: 212008: 82009: 172010: 142011: 102012: 192013: 722014: 472015: 622016: 542017: 902018: 6172019: 962020: 1302021: 1622022: 1552023: 1622024: 2702025: 239
2007high 617 (2018) · low 8 (2008)2025

MAUDE reports naming product code DXN, 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
200727118021
2008238218
20094673317
20104394014
20113472110
201236116019
201334150172
201429133047
20153097062
201630144154
201733184090
2018222350617
201933156196
2020241980130
2021231900162
2022251370155
2023351820162
2024171073270
2025281420239
2026291470—

What is it indicated for?

The Globalcare GUS610 Automatic Blood Pressure Monitor is indicated for home use for the non-invasive measurement of diastolic and systolic blood pressures and pulse rate of adults by means of an inflatable cuff which is wrapped around the upper arm. The cuff circumference is limited to 22 to 42 cm.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K222160: GUS610 Blood pressure monitor.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K222160

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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