510(k) Report

510(k) · Cleared

Cleared

Hypertension Management Software Claient Server (HMS-CS)

K110603510(k) TraditionalCleared Dec 16, 2011288-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

I.E.M. GmbH · DXN System, Measurement, Blood-Pressure, Non-Invasive

Cleared on Dec 16, 2011 as substantially equivalent to K072446 (I.E.M. GmbH, 2007) and 1 other predicate after a 288-day review. Its family tree reaches back 5 generations to 1995. 8 later devices descend from it.

Decided
Dec 16, 2011
Review
288 days
Class
Class II
Product code
DXN
Recalls
None
Predicates
2

Its longest line of descent runs back 5 generations to K950779 (1995). 12 ancestors in all, the oldest K855127 (1986). 8 later devices descend from it, 3 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2007: 1 other ancestor2002: 1 other ancestor2001: 2 other ancestors1999: 1 other ancestor1998: 1 other ancestor1986: 1 other ancestor2012: 1 descendant cleared2014: 2 descendants cleared2016: 2 descendants cleared2021: 1 descendant cleared2026: 2 descendants clearedK950779 · Heart Rate Variability Software Option · Spacelabs, Inc. · 1995K972991 · Monitor One NDX · Qmed, Inc. · 1998K991831 · BMT Anscore Health Management System, Model 1.1 · Boston Medical Technologies, Inc. · 1999K993875 · BMT Anscore Health Management System · Boston Medical Technologies, Inc. · 2000K070795 · Sphygmocor Cardiovascular Management System · Atcor Medical Pty, Ltd. · 20071990200020102020
Other ancestors, by generationDescendants, by generation 1 generation back: 1 other ancestor2 generations back: 3 other ancestors3 generations back: 3 other ancestors 1 generation forward: 3 descendants2 generations forward: 2 descendants3 generations forward: 2 descendants4 generations forward: 1 descendant K070795 · Sphygmocor Cardiovascular Management System · Atcor Medical Pty, Ltd. · 2007K993875 · BMT Anscore Health Management System · Boston Medical Technologies, Inc. · 2000K991831 · BMT Anscore Health Management System, Model 1.1 · Boston Medical Technologies, Inc. · 1999K972991 · Monitor One NDX · Qmed, Inc. · 1998K950779 · Heart Rate Variability Software Option · Spacelabs, Inc. · 1995−50
  1. Root · 5 generations backK950779 Heart Rate Variability Software OptionSpacelabs, Inc. · 1995
  2. 4 generations backK972991 Monitor One NDXQmed, Inc. · 1998
  3. 3 generations backK991831 BMT Anscore Health Management System, Model 1.1Boston Medical Technologies, Inc. · 1999
  4. 2 generations backK993875 BMT Anscore Health Management SystemBoston Medical Technologies, Inc. · 2000
  5. 1 generation backK070795 Sphygmocor Cardiovascular Management SystemAtcor Medical Pty, Ltd. · 2007
  6. This deviceK110603 Hypertension Management Software Claient Server (HMS-CS)I.E.M. GmbH · 2011
  7. Descendant · cites it directly · 5 of its ownK140928 ABPM7100I.E.M. GmbH · 2014
  8. Descendant · 2 generations on · 3 of its ownK151520 Oscar 2Suntech Medical, Inc. · 2016 · Recalled
  9. Descendant · 3 generations on · 1 of its ownK210139 Ambulatory Blood Pressure Monitor, Models: SA-10, SA-05, SA-06…Edan Instruments, Inc. · 2021
  10. Descendant · 3 generations on · 0 of its ownK251581 Wearable Ambulatory Blood Pressure Monitor (WBP-02A)Shenzhen Hingmed Medical Instrument Co., Ltd. · 2026
  11. Descendant · 4 generations on · 0 of its ownK251591 Holter ECG and ABP system (HolterABP)Edan Instruments, Inc. · 2026

Showing 5 of 8 descendants. See all descendants

Descendants cleared per year

2012: 12014: 22016: 22021: 12026: 2
2012high 2 (2014) · low 0 (2013)2026

Most influential descendants

Showing 5 of 8 · See all
  • K140928ABPM7100I.E.M. GmbH · 2014 · cites it directly5descendants
  • K151520Oscar 2Suntech Medical, Inc. · 2016 · 2 generations on3descendants
  • K210139Ambulatory Blood Pressure Monitor, Models: SA-10, SA-05, SA-06, SA-08 and SA-09Edan Instruments, Inc. · 2021 · 3 generations on1descendant
  • K251581Wearable Ambulatory Blood Pressure Monitor (WBP-02A)Shenzhen Hingmed Medical Instrument Co., Ltd. · 2026 · 3 generations on0descendants
  • K251591Holter ECG and ABP system (HolterABP)Edan Instruments, Inc. · 2026 · 4 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−5K950779Heart Rate Variability Software OptionSpacelabs, Inc.1995—
−4K972991Monitor One NDXQmed, Inc.1998—
−3K991831BMT Anscore Health Management System, Model 1.1Boston Medical Technologies, Inc.1999—
−2K993875BMT Anscore Health Management SystemBoston Medical Technologies, Inc.2000—
−1K070795Sphygmocor Cardiovascular Management SystemAtcor Medical Pty, Ltd.2007—
0 (this device)K110603Hypertension Management Software Claient Server (HMS-CS)I.E.M. GmbH2011—
+1K140928ABPM7100I.E.M. GmbH2014—
+2K151520Oscar 2Suntech Medical, Inc.20162
+3K210139Ambulatory Blood Pressure Monitor, Models: SA-10, SA-05, SA-06, SA-08 and SA-09Edan Instruments, Inc.2021—
+3K251581Wearable Ambulatory Blood Pressure Monitor (WBP-02A)Shenzhen Hingmed Medical Instrument Co., Ltd.2026—
+4K251591Holter ECG and ABP system (HolterABP)Edan Instruments, Inc.2026—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198610
199810
199910
200120
200210
200710

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201210
201420
201620
202110
202620
FIG. 1 — Lineage of K110603, 1995–2026Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Get the monthly Device Review Tracker

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
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
*K072446Mobil-O-Graph NG 24 H Abp-Control
Summary page 1
…poiem.de C. Legally Marketed Predicate Devices Predicate 1 The Mobil-C-Graph 24h PWA is substantially equivalent to the Mobil-C-Graph New Generation (Mobil-C-Graph NG, K072446). Predicate 2 The Mobil-C-Graph 24h PWA's Pulse Wave Analysis (PWA) feature as realized through the combination of Mobil-a-Graph…
I.E.M. GmbH2007—
*K070795Sphygmocor Cardiovascular Management System
Summary page 1
…as realized through the combination of Mobil-a-Graph 24h PWA and Hypertension Management Software Client Server (HMS-CS) is substantially equivalent to: SphvpmoCor CvMS (K070795) D. Device Description The Mobil-C-Graph 24h PWA is a modified version of the Mobil-C-Graph New Generation (K072446). Hardware,…
Atcor Medical Pty, Ltd.2007—

What descends from it? (8)

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

NumberDeviceApplicantDecidedDescendants
K140928ABPM7100I.E.M. GmbH20145
K131916Bprosoft Casp PC SoftwareHealthstats International Pte., Ltd.20140
K121266CardioscopePulsecor Limited20120

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 16 years and passes through 5 companies; a new generation was cleared every 3.6 years on median.
  • None of the 12 ancestors has a recall.
  • Of its descendants, K140928 (I.E.M. GmbH, 2014) has gone furthest, with 5 descendants of its own.

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. 2011, 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 Mobil-C-Graph 24h PWA system featuring PWA is an automated microprocessor controlled ambulatory blood pressure monitor (ABPM) which monitors, accumulates and stores: heart beat (rate), systolic and diastolic data of an individual adult patient (in the patient's environment) for a session which may last 24 hours. The Mobil-C-Graph 24h PWA in combination with Hypertension Management Software Client Server (HMS-CS) provides a derived ascending aortic…

Read the full statement (138 words)

The Mobil-C-Graph 24h PWA system featuring PWA is an automated microprocessor controlled ambulatory blood pressure monitor (ABPM) which monitors, accumulates and stores: heart beat (rate), systolic and diastolic data of an individual adult patient (in the patient's environment) for a session which may last 24 hours.

The Mobil-C-Graph 24h PWA in combination with Hypertension Management Software Client Server (HMS-CS) provides a derived ascending aortic blood pressure waveform and a range of central arterial indices. Use of the Augmentation Index ANx only is restricted to patients of age 40 and above.

It is used with a standard cuff blood pressure measurement.

It is used in those patients where information related to the ascending aortic blood pressure is desired but in the opinion of the physician, the risk of cardiac catheterization procedure or other invasive monitoring may outweigh the benefits.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K110603: Hypertension Management Software Claient Server (HMS-CS).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K110603

Report an extraction error

Tell us what is wrong; we check it against the FDA summary.

Are you the manufacturer?

Send a correction or an update to this page, for example a newer model or a public statement about a recall.

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