510(k) Report

510(k) · Cleared

Cleared

Microlife Upper Arm Automatic Digital Blood Pressure Monitor

K202729510(k) TraditionalCleared Apr 8, 2021202-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

Microlife Intellectual Property GmbH · DXN System, Measurement, Blood-Pressure, Non-Invasive

Cleared on Apr 8, 2021 as substantially equivalent to K200297 (Microlife Intellectual Property GmbH, 2020) and 1 other predicate after a 202-day review. Its family tree reaches back 11 generations to 1991.

Decided
Apr 8, 2021
Review
202 days
Class
Class II
Product code
DXN
Recalls
None
Predicates
2

Its longest line of descent runs back 11 generations to K903134 (1991). 36 ancestors in all, the oldest K872291 (1987). No later device cites it as a predicate yet.

Other ancestors, by year cleared 2008: 2 other ancestors2002: 5 other ancestors2001: 3 other ancestors1993: 2 other ancestors2014: 1 other ancestor2006: 2 other ancestors1999: 2 other ancestors1998: 2 other ancestors1997: 2 other ancestors1996: 1 other ancestor1995: 1 other ancestor1992: 1 other ancestor1987: 1 other ancestorK903134 · Omron Auto Oscillometric Dig BP Mont/Hem-704C 705C · Omron Marshall Products, Inc. · 1991K970211 · Microlife Automatic Blood Pressure Monitor · Micro Weiss Electronics · 1998K013485 · Microlife Upper Arm Automatic Blood Pressure Monitor, Model BP-3BTO-1, with Optional Thermal Printer, Model PR 1KA1 · Microlife Corp. · 2002K041411 · Microlife Upper Arm Blood Pressure Monitor, Model BP-3BTO-AP · Microlife Corp. · 2004K060686 · Microlife Automatic Blood Pressure Monitor, Model BP3AC1-1PC · Microlife Intellectual Property GmbH · 2006K073198 · Microlife Upper Arm Automatic Digital Blood Pressure Monitor, Model Watchbp Home (BP3MX1-1) · Microlife Intellectual Property GmbH · 2008K082357 · Microlife Upper Arm Automatic Digital Blood Pressure Monitor, Modelwatchbp Office (TWIN200). · Microlife Intellectual Property GmbH · 2008K101275 · Microlife Upper Arm Automatic Digital Blood Pressure Monitor, Watch BP Office Afib (TWIN200 Afs). · Microlife Intellectual Property GmbH · 2010K143341 · Microlife Upper Arm Automatic Digital Blood Pressure Monitor · Microlife Intellectual Property GmbH · 2015K152770 · ProBP 2400 Digital Blood Pressure Device · Microlife Intellectual Property GmbH · 2015 · recalledK200297 · Microlife Upper Arm Automatic Digital Blood Pressure Monitor · Microlife Intellectual Property GmbH · 20201990200020102020
Other ancestors, by generation 1 generation back: 1 other ancestor2 generations back: 1 other ancestor3 generations back: 2 other ancestors4 generations back: 1 other ancestor5 generations back: 3 other ancestors6 generations back: 3 other ancestors7 generations back: 8 other ancestors8 generations back: 6 other ancestors K200297 · Microlife Upper Arm Automatic Digital Blood Pressure Monitor · Microlife Intellectual Property GmbH · 2020K152770 · ProBP 2400 Digital Blood Pressure Device · Microlife Intellectual Property GmbH · 2015 · recalledK143341 · Microlife Upper Arm Automatic Digital Blood Pressure Monitor · Microlife Intellectual Property GmbH · 2015K101275 · Microlife Upper Arm Automatic Digital Blood Pressure Monitor, Watch BP Office Afib (TWIN200 Afs). · Microlife Intellectual Property GmbH · 2010K082357 · Microlife Upper Arm Automatic Digital Blood Pressure Monitor, Modelwatchbp Office (TWIN200). · Microlife Intellectual Property GmbH · 2008K073198 · Microlife Upper Arm Automatic Digital Blood Pressure Monitor, Model Watchbp Home (BP3MX1-1) · Microlife Intellectual Property GmbH · 2008K060686 · Microlife Automatic Blood Pressure Monitor, Model BP3AC1-1PC · Microlife Intellectual Property GmbH · 2006K041411 · Microlife Upper Arm Blood Pressure Monitor, Model BP-3BTO-AP · Microlife Corp. · 2004K013485 · Microlife Upper Arm Automatic Blood Pressure Monitor, Model BP-3BTO-1, with Optional Thermal Printer, Model PR 1KA1 · Microlife Corp. · 2002K970211 · Microlife Automatic Blood Pressure Monitor · Micro Weiss Electronics · 1998K903134 · Omron Auto Oscillometric Dig BP Mont/Hem-704C 705C · Omron Marshall Products, Inc. · 1991−10−50
  1. Root · 11 generations backK903134 Omron Auto Oscillometric Dig BP Mont/Hem-704C 705COmron Marshall Products, Inc. · 1991
  2. 7 generations between
  3. 3 generations backK143341 Microlife Upper Arm Automatic Digital Blood Pressure MonitorMicrolife Intellectual Property GmbH · 2015
  4. 2 generations backK152770 ProBP 2400 Digital Blood Pressure DeviceMicrolife Intellectual Property GmbH · 2015 · Recalled
  5. 1 generation backK200297 Microlife Upper Arm Automatic Digital Blood Pressure MonitorMicrolife Intellectual Property GmbH · 2020
  6. This deviceK202729 Microlife Upper Arm Automatic Digital Blood Pressure MonitorMicrolife Intellectual Property GmbH · 2021
Show all 11 generations
  1. Root · 11 generations backK903134 Omron Auto Oscillometric Dig BP Mont/Hem-704C 705COmron Marshall Products, Inc. · 1991
  2. 10 generations backK970211 Microlife Automatic Blood Pressure MonitorMicro Weiss Electronics · 1998
  3. 9 generations backK013485 Microlife Upper Arm Automatic Blood Pressure Monitor, Model…Microlife Corp. · 2002
  4. 8 generations backK041411 Microlife Upper Arm Blood Pressure Monitor, Model BP-3BTO-APMicrolife Corp. · 2004
  5. 7 generations backK060686 Microlife Automatic Blood Pressure Monitor, Model BP3AC1-1PCMicrolife Intellectual Property GmbH · 2006
  6. 6 generations backK073198 Microlife Upper Arm Automatic Digital Blood Pressure Monitor, Model…Microlife Intellectual Property GmbH · 2008
  7. 5 generations backK082357 Microlife Upper Arm Automatic Digital Blood Pressure Monitor…Microlife Intellectual Property GmbH · 2008
  8. 4 generations backK101275 Microlife Upper Arm Automatic Digital Blood Pressure Monitor, Watch…Microlife Intellectual Property GmbH · 2010
  9. 3 generations backK143341 Microlife Upper Arm Automatic Digital Blood Pressure MonitorMicrolife Intellectual Property GmbH · 2015
  10. 2 generations backK152770 ProBP 2400 Digital Blood Pressure DeviceMicrolife Intellectual Property GmbH · 2015 · Recalled
  11. 1 generation backK200297 Microlife Upper Arm Automatic Digital Blood Pressure MonitorMicrolife Intellectual Property GmbH · 2020
  12. This deviceK202729 Microlife Upper Arm Automatic Digital Blood Pressure MonitorMicrolife Intellectual Property GmbH · 2021
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−11K903134Omron Auto Oscillometric Dig BP Mont/Hem-704C 705COmron Marshall Products, Inc.1991—
−10K970211Microlife Automatic Blood Pressure MonitorMicro Weiss Electronics1998—
−9K013485Microlife Upper Arm Automatic Blood Pressure Monitor, Model BP-3BTO-1, with…Microlife Corp.2002—
−8K041411Microlife Upper Arm Blood Pressure Monitor, Model BP-3BTO-APMicrolife Corp.2004—
−7K060686Microlife Automatic Blood Pressure Monitor, Model BP3AC1-1PCMicrolife Intellectual Property GmbH2006—
−6K073198Microlife Upper Arm Automatic Digital Blood Pressure Monitor, Model Watchbp…Microlife Intellectual Property GmbH2008—
−5K082357Microlife Upper Arm Automatic Digital Blood Pressure Monitor, Modelwatchbp…Microlife Intellectual Property GmbH2008—
−4K101275Microlife Upper Arm Automatic Digital Blood Pressure Monitor, Watch BP Office…Microlife Intellectual Property GmbH2010—
−3K143341Microlife Upper Arm Automatic Digital Blood Pressure MonitorMicrolife Intellectual Property GmbH2015—
−2K152770ProBP 2400 Digital Blood Pressure DeviceMicrolife Intellectual Property GmbH20151
−1K200297Microlife Upper Arm Automatic Digital Blood Pressure MonitorMicrolife Intellectual Property GmbH2020—
0 (this device)K202729Microlife Upper Arm Automatic Digital Blood Pressure MonitorMicrolife Intellectual Property GmbH2021—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198710
199210
199320
199510
199610
199720
199820
199920
200130
200250
200620
200820
201410
FIG. 1 — Lineage of K202729, 1991–2021Source: 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
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
*K200297Microlife Upper Arm Automatic Digital Blood Pressure Monitor
Summary page 4
…eared Device (Predicate Device): Primary Predicate: Microlife Upper Arm Automatic Digital Blood Pressure Monitor, Model WatchBP Office (BP3SK1-3B), K200297, Microlife Intellectual Property GmbH. Reference Predicate: Microlife Upper Arm Automatic Digital Blood Pressure…
Microlife Intellectual Property GmbH2020—
*K082881Microlife Upper Arm Automatic Digital Blood Pressure Monitor, Model Watchbp O3
Summary page 4
…rolife Intellectual Property GmbH. Reference Predicate: Microlife Upper Arm Automatic Digital Blood Pressure Monitor, Model WatchBP 03 (BP3MZ1-1), K082881, Microlife Intellectual Property GmbH. Page 1 of 8…
Microlife Intellectual Property GmbH2008—

Also cleared against K200297: 1 other device →

What descends from it?

No later submission names this one as a predicate yet.

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 30 years and passes through 4 companies; a new generation was cleared every 1.9 years on median.
  • 1 of the 36 ancestors has a recall of any class.
  • 1 other device also cites its predicate K200297.

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. 2021, 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 Microlife Upper Arm Automatic Digital Blood Pressure Monitor,Model WatchBP 03 (BP3SZl-1) is a non-invasive 24 hour ambulatory blood pressure monitor (ABPM) using oscillometric technique and an upper-arm blood pressure cuff to measure systolic and diastolic blood pressures, pulse rate, mean arterial pressure (MAP) for or use in adults and pediatrics (but not neonates) with arm cuff circumference sizes ranging from 14 -52 cm. The device can accurately…

Read the full statement (181 words)

The Microlife Upper Arm Automatic Digital Blood Pressure Monitor,Model WatchBP 03 (BP3SZl-1) is a non-invasive 24 hour ambulatory blood pressure monitor (ABPM) using oscillometric technique and an upper-arm blood pressure cuff to measure systolic and diastolic blood pressures, pulse rate, mean arterial pressure (MAP) for or use in adults and pediatrics (but not neonates) with arm cuff circumference sizes ranging from 14 -52 cm.

The device can accurately measure blood pressure in pregnant patients including those with known or suspected pre-eclampsia.

The device provides aortic blood pressure parameters, includes central systolic blood pressure (cSBP), central pulse pressure (cPP) and central diastolic blood pressure (cDBP), non-invasively through the use of a brachial cuff.

The device detects the appearance of atrial fibrillation during measurement and gives a warning signal together with the measured blood pressure value if atrial fibrillation is detected.

The memory data can be transferred to the PC (personal computer) running the WatchBP Analyzer software by connecting the monitor via USB cable or Bluetooth.

The device is intended to be used by healthcare professionals and patients in clinical and patient's environments.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K202729: Microlife Upper Arm Automatic Digital Blood Pressure Monitor.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K202729

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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