# K123020: Blip Model BP-700WF

- Pathway: 510(k) (Special)
- Applicant: Carematix, Inc.
- Decided: Nov 28, 2012 after 61 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
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
BP 700-WF is a non-invasive blood pressure measurement device intended to measure systolic, diastolic blood pressure and pulse rate of an adult individual over age 15, at home by using a non-invasive technique in which an inflatable cuff is wrapped around the upper arm. The cuff circumference is limited to 9"-13" for Arm type. The device can transmit the readings through wireless communication for record archiving and review.

Source page: https://510kreport.com/device/K123020
Methodology: https://510kreport.com/methodology