# K090664: Devon Accubp Cuff

- Pathway: 510(k) (Traditional)
- Applicant: Devon Medical, Inc.
- Decided: Mar 23, 2009 after 10 days
- Product code: DXQ (Blood Pressure Cuff)
- Device class: 2
- Regulation: 21 CFR 870.1120
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K071244 (2008). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K071244: Medline Single Patient Use Blood Pressure Cuff, Medline Industries, Inc. (2008) Summary page 1.

## Indications for use
The Devon AccuBP Cuff is intended to be used in conjunction with non-invasive blood pressure monitoring systems for determination of a person's blood pressure. The device is non-sterile and disposable. It is available in neonatal, through adult sizes.

Source page: https://510kreport.com/device/K090664
Methodology: https://510kreport.com/methodology