# K101512: Microlife Upper Arm Automatic Digital Blood Pressure Monitor, Watchbp Office Target (BP3MD1-4).

- Pathway: 510(k) (Special)
- Applicant: Microlife Intellectual Property GmbH
- Decided: Jul 1, 2010 after 30 days
- Product code: DXN (System, Measurement, Blood-Pressure, Non-Invasive)
- Device class: 2
- Regulation: 21 CFR 870.1130
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 7 generations back to K903134 (1991). 17 ancestors in all.
No later device cites it as a predicate yet.
0 of 18 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K013485: Microlife Upper Arm Automatic Blood Pressure Monitor, Model BP-3BTO-1, with Optional Thermal Printer, Model PR 1KA1, Microlife Corp. (2002) Summary page 1.
- K082357: Microlife Upper Arm Automatic Digital Blood Pressure Monitor, Modelwatchbp Office (TWIN200)., Microlife Intellectual Property GmbH (2008) Summary page 1.

## Indications for use
The Microlife Upper Arm Automatic Digital Blood Pressure Monitor, Model WatchBP Office Target (BP3MD1-4) is a device intended to measure the systolic and diastolic blood pressure, pulse rate and pulse pressure (PR) of an adult individual by using a non-invasive oscillometric technique in which an inflatable cuff is wrapped around the upper arm.

Source page: https://510kreport.com/device/K101512
Methodology: https://510kreport.com/methodology