510(k) · Cleared
ClearedAmplief Wrist Blood Pressure Monitor, Model M600
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Amplife Corporation · DXN System, Measurement, Blood-Pressure, Non-Invasive
Cleared on Mar 4, 2005 as substantially equivalent to K040002 (Microlife Intellectual Property Gmb, 2004) after a 14-day review. Its family tree reaches back 2 generations to 2002.
- Decided
- Mar 4, 2005
- Review
- 14 days
- Class
- Class II
- Product code
- DXN
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 2 generations to K021305 (2002). No later device cites it as a predicate yet.
- Root · 2 generations backK021305 Microlife Wrist Watch Blood Pressure, Model BP-3BU1-5, with Optional…Microlife Corp. · 2002
- 1 generation backK040002 Microlife Wrist Watch Blood Pressure Monitor, Model BP3AX1Microlife Intellectual Property Gmb · 2004
- This deviceK050413 Amplief Wrist Blood Pressure Monitor, Model M600Amplife Corporation · 2005
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −2 | K021305 | Microlife Wrist Watch Blood Pressure, Model BP-3BU1-5, with Optional Thermal… | Microlife Corp. | 2002 | — |
| −1 | K040002 | Microlife Wrist Watch Blood Pressure Monitor, Model BP3AX1 | Microlife Intellectual Property Gmb | 2004 | — |
| 0 (this device) | K050413 | Amplief Wrist Blood Pressure Monitor, Model M600 | Amplife Corporation | 2005 | — |
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 K222125 Arm Blood Pressure Monitor, models AOJ-30A…score 18.5 · 8 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
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.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K040002 | Microlife Wrist Watch Blood Pressure Monitor, Model BP3AX1Summary page 1…atch Automatic Blood Pressure Monitor, Model M600 is substantially equivalent to the Microlife Automatic Wrist Watch Blood Pressure Monitor, Model BP3AX1, K# 040002. 4. Device Description: The AMPLIFE Wrist Watch Automatic Blood Pressure Monitor, Model M600 is designed to meas… | 2004 |
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 3 years and passes through 3 companies; a new generation was cleared every 1.7 years on median.
- None of the 2 ancestors has a recall.
- 3 other devices also cite its predicate K040002.
How does its category compare?
All DXN devicesDXN System, Measurement, Blood-Pressure, Non-Invasive: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · DXN
28in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · DXN
142in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · DXN
3in 2024
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · DXN
239in 2025
MAUDE reports naming product code DXN, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 27 | 118 | 0 | 21 |
| 2008 | 23 | 82 | 1 | 8 |
| 2009 | 46 | 73 | 3 | 17 |
| 2010 | 43 | 94 | 0 | 14 |
| 2011 | 34 | 72 | 1 | 10 |
| 2012 | 36 | 116 | 0 | 19 |
| 2013 | 34 | 150 | 1 | 72 |
| 2014 | 29 | 133 | 0 | 47 |
| 2015 | 30 | 97 | 0 | 62 |
| 2016 | 30 | 144 | 1 | 54 |
| 2017 | 33 | 184 | 0 | 90 |
| 2018 | 22 | 235 | 0 | 617 |
| 2019 | 33 | 156 | 1 | 96 |
| 2020 | 24 | 198 | 0 | 130 |
| 2021 | 23 | 190 | 0 | 162 |
| 2022 | 25 | 137 | 0 | 155 |
| 2023 | 35 | 182 | 0 | 162 |
| 2024 | 17 | 107 | 3 | 270 |
| 2025 | 28 | 142 | 0 | 239 |
| 2026 | 29 | 147 | 0 | — |
What is it indicated for?
The AMPLIFE Wrist Watch Blood Pressure Monitor, Model M600 is a device intended to measure the systolic and diastolic blood pressure and pulse rate of an adult individual by using a non-invasive technique in which an inflatable cuff is wrapped around the wrist.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K050413 · printed Nov 3, 2026
Cite this page
510(k) Report. “K050413: Amplief Wrist Blood Pressure Monitor, Model M600.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 3, 2026. https://510kreport.com/device/K050413
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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