# K002530: Welch Allyn Spot Check Device

- Pathway: 510(k) (Abbreviated)
- Applicant: Welch Allyn, Inc.
- Decided: Nov 14, 2000 after 90 days
- Product code: DXN (System, Measurement, Blood-Pressure, Non-Invasive)
- Device class: 2
- Regulation: 21 CFR 870.1130
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
100 later devices descend from it; 3 cite it directly.
0 of 101 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
- K040490: Welch Allyn Spot Ultra Vital Signs Device (2004), 97 descendants of its own
- K093907: Welch Allyn Non Invasive Blood Pressure (Nibp) Device (2010), 74 descendants of its own
- K101445: Vital Signs Monitor-VSM 6000 Series (2010), 73 descendants of its own
- K110516: Connex Vital Signs Monitor 6000 Series (2011), 67 descendants of its own
- K112687: Connex (R) Vital Signs Monitor 6000 Series (2011), 66 descendants of its own

Source page: https://510kreport.com/device/K002530
Methodology: https://510kreport.com/methodology