# K012746: Ice Baton

- Pathway: 510(k) (Traditional)
- Applicant: Behive, Ltd.
- Decided: Nov 14, 2001 after 90 days
- Product code: LKX (Device, Thermal, Hemorrhoids)
- Device class: U
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K981428 (1998). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K981428: Anu Ice, Cryoptherapy Pain Relief Products, Inc. (1998) Summary page 1.

## Indications for use
The Ice Baton is intended to provide relief from pain and discomfort due to hemorthoids

Source page: https://510kreport.com/device/K012746
Methodology: https://510kreport.com/methodology