# K022482: Sensa-Cuff, Models Infant, Child, Adult

- Pathway: 510(k) (Traditional)
- Applicant: Ge Medical Systems Information Technologies
- Decided: Aug 13, 2002 after 15 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
No predicates in its family tree.
35 later devices descend from it; 6 cite it directly.
0 of 36 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) DURA-CUFB-Preamendment: named in the summary without a submission number

## Most influential descendants
- K112544: Unimed Blood Pressure Cuff (2011), 24 descendants of its own
- K151290: Disposable Blood Pressure Cuff, Reusable Blood Pressure Cuff (2015), 9 descendants of its own
- K182433: Reusable Blood Pressure Cuff, Disposable Blood Pressure Cuff (2018), 7 descendants of its own
- K152468: Reusable Blood Pressure Cuff (2015), 4 descendants of its own
- K120125: Soft-Cuf, Classic-Cuf, Dura-Cuf, Sensa-Cuf (2012), 3 descendants of its own

## Indications for use
The Sensa-Cuff Blood Pressure Cuff is an accessory used in conjunction with noninvasive blood measurement systems. The cuff is non-sterile and may be reused. It is available in pediatric and adult sizes. The cuff is not designed, sold, or intended for use except as indicated.

Source page: https://510kreport.com/device/K022482
Methodology: https://510kreport.com/methodology