# K002372: Access Alert Gauge

- Pathway: 510(k) (Traditional)
- Applicant: Medisystems Corp.
- Decided: Oct 25, 2000 after 82 days
- Product code: KOC (Accessories, Blood Circuit, Hemodialysis)
- Device class: 2
- Regulation: 21 CFR 876.5820
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
6 later devices descend from it; 1 cites it directly.
0 of 7 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
- K030456: Vasc-Alert (2003), 5 descendants of its own
- K042566: Vasc-Alert (2004), 4 descendants of its own
- K093834: Crit-Line Anemia Management Software (2010), 3 descendants of its own
- K130579: Physoft Ams (2013), 2 descendants of its own
- K232283: PhySoftAMS® (2023), 0 descendants of its own

Source page: https://510kreport.com/device/K002372
Methodology: https://510kreport.com/methodology