# K902269: Electri-Cool (TM) Liquid-Circulat. Thermal Therapy

- Pathway: 510(k) (Traditional)
- Applicant: Seabrook Medical Systems, Inc.
- Decided: Jun 21, 1990 after 31 days
- Product code: ILO (Pack, Hot Or Cold, Water Circulating)
- Device class: 2
- Regulation: 21 CFR 890.5720
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 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
- K955529: Crytron System (1996), 0 descendants of its own

## Recalls of this device
- Jan 7, 2015 · Class II · Z-1129-2015: Seals in the water path of the CT-99 cold therapy pad may separate during use, which could lead to a water leak.

Source page: https://510kreport.com/device/K902269
Methodology: https://510kreport.com/methodology