510(k) Report

510(k) · Cleared

Cleared

Microlife Upper Arm Automatic Digital Blood Pressure Monitor

K153077510(k) TraditionalCleared Feb 12, 2016112-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 Feb 12, 2016 as substantially equivalent to K140572 (Microlife Intellectual Property GmbH, Switzerland, 2014) and 1 other predicate after a 112-day review. Its family tree reaches back 8 generations to 1991. 12 later devices descend from it.

Decided
Feb 12, 2016
Review
112 days
Class
Class II
Product code
DXN
Recalls
None
Predicates
2

Its longest line of descent runs back 8 generations to K903134 (1991). 21 ancestors in all, the oldest K872291 (1987). 12 later devices descend from it, 4 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2014: 1 other ancestor2006: 1 other ancestor2002: 3 other ancestors1999: 1 other ancestor1998: 2 other ancestors1997: 1 other ancestor1993: 1 other ancestor1996: 1 other ancestor1995: 1 other ancestor1987: 1 other ancestor2023: 3 descendants cleared2020: 1 descendant cleared2017: 1 descendant cleared2019: 1 descendant cleared2024: 2 descendants cleared2025: 1 descendant cleared2026: 3 descendants clearedReference device: K111652 · Microlife Automatic Talking Blood Pressure Monitor · Microlife Intellectual Property GmbH · 2011K903134 · 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 · 2008K151869 · Microlife Upper Arm Automatic Digital Blood Pressure Monitor · Microlife Intellectual Property GmbH, Switzerland · 20151990200020102020
  1. Root · 8 generations backK903134 Omron Auto Oscillometric Dig BP Mont/Hem-704C 705COmron Marshall Products, Inc. · 1991
  2. 7 generations backK970211 Microlife Automatic Blood Pressure MonitorMicro Weiss Electronics · 1998
  3. 6 generations backK013485 Microlife Upper Arm Automatic Blood Pressure Monitor, Model…Microlife Corp. · 2002
  4. 5 generations backK041411 Microlife Upper Arm Blood Pressure Monitor, Model BP-3BTO-APMicrolife Corp. · 2004
  5. 4 generations backK060686 Microlife Automatic Blood Pressure Monitor, Model BP3AC1-1PCMicrolife Intellectual Property GmbH · 2006
  6. 3 generations backK073198 Microlife Upper Arm Automatic Digital Blood Pressure Monitor, Model…Microlife Intellectual Property GmbH · 2008
  7. 2 generations backK082357 Microlife Upper Arm Automatic Digital Blood Pressure Monitor…Microlife Intellectual Property GmbH · 2008
  8. 1 generation backK151869 Microlife Upper Arm Automatic Digital Blood Pressure MonitorMicrolife Intellectual Property GmbH, Switzerland · 2015
  9. This deviceK153077 Microlife Upper Arm Automatic Digital Blood Pressure MonitorMicrolife Intellectual Property GmbH · 2016
  10. Descendant · cites it directly · 5 of its ownK222979 Microlife Upper Arm Automatic Digital Blood Pressure Monitor, Model…Microlife Intellectual Property GmbH · 2023
  11. Descendant · 2 generations on · 3 of its ownK232621 Blood pressure monitorGuangdong Transtek Medical Electronics Co., Ltd. · 2023
  12. Descendant · cites it directly · 3 of its ownK172498 Microlife Upper Arm Automatic Digital Blood Pressure Monitor, Model…Microlife Intellectual Property GmbH · 2017
  13. Descendant · 2 generations on · 2 of its ownK230075 Microlife Upper Arm Automatic Digital Blood Pressure Monitor, Model…Microlife Intellectual Property GmbH · 2023
  14. Descendant · 3 generations on · 1 of its ownK251120 Microlife Upper Arm Automatic Digital Blood Pressure Monitor, Model…Microlife Corporation · 2025

Showing 5 of 12 descendants. See all descendants

Descendants cleared per year

2017: 12019: 12020: 12023: 32024: 22025: 12026: 3
2017high 3 (2023) · low 0 (2018)2026

Most influential descendants

Showing 5 of 12 · See all
  • K222979Microlife Upper Arm Automatic Digital Blood Pressure Monitor, Model BP3KV1-5WMicrolife Intellectual Property GmbH · 2023 · cites it directly5descendants
  • K232621Blood pressure monitorGuangdong Transtek Medical Electronics Co., Ltd. · 2023 · 2 generations on3descendants
  • K172498Microlife Upper Arm Automatic Digital Blood Pressure Monitor, Model BP3MW1-4YMicrolife Intellectual Property GmbH · 2017 · cites it directly3descendants
  • K230075Microlife Upper Arm Automatic Digital Blood Pressure Monitor, Model BP3KVl-5KMicrolife Intellectual Property GmbH · 2023 · 2 generations on2descendants
  • K251120Microlife Upper Arm Automatic Digital Blood Pressure Monitor, Model BP Progress…Microlife Corporation · 2025 · 3 generations on1descendant
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−8K903134Omron Auto Oscillometric Dig BP Mont/Hem-704C 705COmron Marshall Products, Inc.1991—
−7K970211Microlife Automatic Blood Pressure MonitorMicro Weiss Electronics1998—
−6K013485Microlife Upper Arm Automatic Blood Pressure Monitor, Model BP-3BTO-1, with…Microlife Corp.2002—
−5K041411Microlife Upper Arm Blood Pressure Monitor, Model BP-3BTO-APMicrolife Corp.2004—
−4K060686Microlife Automatic Blood Pressure Monitor, Model BP3AC1-1PCMicrolife Intellectual Property GmbH2006—
−3K073198Microlife Upper Arm Automatic Digital Blood Pressure Monitor, Model Watchbp…Microlife Intellectual Property GmbH2008—
−2K082357Microlife Upper Arm Automatic Digital Blood Pressure Monitor, Modelwatchbp…Microlife Intellectual Property GmbH2008—
−1K151869Microlife Upper Arm Automatic Digital Blood Pressure MonitorMicrolife Intellectual Property GmbH, Switzerland2015—
0 (this device)K153077Microlife Upper Arm Automatic Digital Blood Pressure MonitorMicrolife Intellectual Property GmbH2016—
+1K222979Microlife Upper Arm Automatic Digital Blood Pressure Monitor, Model BP3KV1-5WMicrolife Intellectual Property GmbH2023—
+2K232621Blood pressure monitorGuangdong Transtek Medical Electronics Co., Ltd.2023—
+1K172498Microlife Upper Arm Automatic Digital Blood Pressure Monitor, Model BP3MW1-4YMicrolife Intellectual Property GmbH2017—
+2K230075Microlife Upper Arm Automatic Digital Blood Pressure Monitor, Model BP3KVl-5KMicrolife Intellectual Property GmbH2023—
+3K251120Microlife Upper Arm Automatic Digital Blood Pressure Monitor, Model BP…Microlife Corporation2025—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198710
199310
199510
199610
199710
199820
199910
200230
200610
201410

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201710
201910
202010
202330
202420
202510
202630
FIG. 1 — Lineage of K153077, 1991–2026Source: 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
*K140572Microlife Upper Arm Automatic Digital Blood Pressure Monitor
Summary page 4
…3. Information for the 510(k) Cleared Device (Predicate Device): a. Microlife Upper Arm Automatic Digital Blood Pressure Monitor, Model BP3MW1-4X(R), K140572, Microlife Intellectual Property GmbH. b. Microlife Upper Arm Automatic Digital Blood Pressure Monitor, Model BP3NF1-…
Microlife Intellectual Property GmbH, Switzerland2014—
*K151869Microlife Upper Arm Automatic Digital Blood Pressure Monitor
Summary page 4
…l BP3MW1-4X(R), K140572, Microlife Intellectual Property GmbH. b. Microlife Upper Arm Automatic Digital Blood Pressure Monitor, Model BP3NF1- 2B, K151869, Microlife Intellectual Property GmbH. 4. Device Description: Microlife Upper Arm Automatic Digital Blood Pressure M…
Microlife Intellectual Property GmbH, Switzerland2015—
†K111652Microlife Automatic Talking Blood Pressure MonitorMicrolife Intellectual Property GmbH2011—

Also cleared against K140572: 1 other device →

What descends from it? (12)

See all 12

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

NumberDeviceApplicantDecidedDescendants
K222979Microlife Upper Arm Automatic Digital Blood Pressure Monitor, Model BP3KV1-5WMicrolife Intellectual Property GmbH20235
K172498Microlife Upper Arm Automatic Digital Blood Pressure Monitor, Model BP3MW1-4YMicrolife Intellectual Property GmbH20173
K200521Full Automatic (NIBP) Blood Pressure MonitorHealth & Life Co., Ltd.20200
K190818Microlife Upper Arm Automatic Digital Blood Pressure MonitorMicrolife Intellectual Property GmbH20190

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 25 years and passes through 5 companies; a new generation was cleared every 2.5 years on median.
  • None of the 21 ancestors has a recall.
  • Of its descendants, K222979 (Microlife Intellectual Property GmbH, 2023) has gone furthest, with 5 descendants of its own.
  • 1 other device also cites its predicate K140572.

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. 2016, 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 BP3MW 1-4B is a device intended to measure the systolic and diastolic blood pressure, pulse rate of an adult individual by using a non-invasive oscillometric technique in one inflatable cuff is wrapped around the single upper arm. The device detects the appearance of irregular heartbeat during measurement, and gives a warning signal with the reading once the irregular heartbeat is…

Read the full statement (154 words)

The Microlife Upper Arm Automatic Digital Blood Pressure Monitor, Model BP3MW 1-4B is a device intended to measure the systolic and diastolic blood pressure, pulse rate of an adult individual by using a non-invasive oscillometric technique in one inflatable cuff is wrapped around the single upper arm.

The device detects the appearance of irregular heartbeat during measurement, and gives a warning signal with the reading once the irregular heartbeat is detected.

This device can accurately measure blood pressure in pregnant patients including those with known or suspected preeclampsia.

The memory data can be transferred to the PC (personal computer) running the Microlife Blood Pressure Analyzer (BPA) software by connecting the monitor via cable. The device can also be used in connection with smart mobile devices running the APP and via Bluetooth.

The blood pressure monitor is a fully automatic digital blood pressure measuring device for use by adults on the upper arm at home.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K153077: 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/K153077

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