# K062238: Tytan Blood Pressure Cuff

- Pathway: 510(k) (Traditional)
- Applicant: Tytan Medical Corp.
- Decided: Sep 21, 2006 after 50 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 K010686 (2001). 2 ancestors in all.
24 later devices descend from it; 1 cites it directly.
0 of 27 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K051539: Tricot Blood Pressure Cuff, Ya Horng Electronic Co., Ltd. (2005) Summary page 3.

## Most influential descendants
- K102825: Blood Pressure Cuff (2011), 23 descendants of its own
- K113623: Patient Monitor (2012), 15 descendants of its own
- K131971: IM60/IM70 Patient Monitor (2014), 14 descendants of its own
- K120173: Patient Monitor (2012), 10 descendants of its own
- K160981: Patient Monitor (2016), 8 descendants of its own

## Indications for use
The TYTAN blood pressure cuff is used in conjunction with non-invasive blood pressure measurement systems by personnel properly trained. The device is non-sterile and is intended as a reusable multi-patient device for measuring one's blood pressure. It is available in newborn through large adult sizes.

Source page: https://510kreport.com/device/K062238
Methodology: https://510kreport.com/methodology