# K061962: Surgi-Cuf Reusable, RS Series

- Pathway: 510(k) (Traditional)
- Applicant: Ethox International
- Decided: Jul 25, 2006 after 13 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: 2 generations back to K883977 (1989). 3 ancestors in all.
No later device cites it as a predicate yet.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K022482: Sensa-Cuff, Models Infant, Child, Adult, Ge Medical Systems Information Technologies (2002) Summary page 2.
- K040286: Ethox Surgi-Cuf Adult Disposable Blood Pressure Cuffs, Ethox Corp. (2004) Summary page 2.
- (no number) Critikon Dura-Cuf: named in the summary without a submission number

## Indications for use
The SURGI-CUF® REUSABLE Blood Pressure Cuff is a bladder and tube set for use in conjunction with a variety of blood pressure monitoring systems for determination of a persons blood pressure. The device is non-sterile and reusable.

Source page: https://510kreport.com/device/K061962
Methodology: https://510kreport.com/methodology