# K883977: Surgi-Cuf Sterile/Non-Sterile Disposable

- Pathway: 510(k) (Traditional)
- Applicant: Ethox Corp.
- Decided: Feb 10, 1989 after 143 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.
54 later devices descend from it; 4 cite it directly.
0 of 55 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K974080: Critikon Soft Blood Pressure Cuff (1998), 51 descendants of its own
- K120364: Unimed Disposable Blood Pressure Cuff (2012), 23 descendants of its own
- K012194: Blood Pressure Monitor (Sphygmomanometer), Model HT-110 (2001), 14 descendants of its own
- K043286: Aneroid Sphygmomanometer, Model BK2002 (2005), 13 descendants of its own
- K173246: Aneroid Sphygmomanometer (2018), 10 descendants of its own

Source page: https://510kreport.com/device/K883977
Methodology: https://510kreport.com/methodology