# K172049: CryoIQ DERM, CryoIQ PRO, CryoIQ EquiMED

- Pathway: 510(k) (Traditional)
- Applicant: Cry IQ AB
- Decided: Aug 30, 2017 after 55 days
- Product code: GEH (Unit, Cryosurgical, Accessories)
- Device class: 2
- Regulation: 21 CFR 878.4350
- 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 K024009 (2003). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K091721: Cryosuccess, Model C-Suc-01, C-Suc-02, C-DTS-02, C-DTS-03, C-GTS-13. C-CA-23, New Medical Technologies GmbH (2009) Summary page 4.

## Indications for use
The CryoIQ Multi LINE are reusable devices intended to destroy tissue during surgical procedures by applying extreme cold.

Source page: https://510kreport.com/device/K172049
Methodology: https://510kreport.com/methodology