# K072752: BP Limbo XL, Bptango XL, BP Salsa XL

- Pathway: 510(k) (Traditional)
- Applicant: Datadancer Medical Systems
- Decided: Oct 31, 2008 after 400 days
- Product code: DQK (Computer, Diagnostic, Programmable)
- Device class: 2
- Regulation: 21 CFR 870.1425
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 5 generations back to K903134 (1991). 7 ancestors in all.
No later device cites it as a predicate yet.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K060686: Microlife Automatic Blood Pressure Monitor, Model BP3AC1-1PC, Microlife Intellectual Property GmbH (2006) Summary page 1.
- K042818: Panasonic Wrist Blood Pressure Monitor, Models EW3003 and EW3037, Matsushita Electric Works, Ltd. (2005) Summary page 1.

## Indications for use
bp Limbo XL, bp Salsa XL and bp Tango XL are designed for Adult Blood Pressure Only or persons 18 years or older. bp Limbo XL, bp Salsa XL and bp Tango XL are intended to be used as a personal blood pressure log to record patient measured results from a personal blood pressure monitor aiding in the management of hypertension as directed by a patient's physician or health care provider. The printed reports, and subsequent information contained within, are intended for review and interpretation by a physician and not as a stand alone diagnostic tool. If bp Limbo XL, bp Salsa XL or bp Tango XL are used without a physician or health care provider relationship, all information must be considered educational, relating to the user's condition, and not as medical advice for the purpose of diagnosis, administration of treatment(s) or to prescribe medication(s).

Source page: https://510kreport.com/device/K072752
Methodology: https://510kreport.com/methodology