# K070135: Vitrifreeze Medium; Vitrithaw Medium

- Pathway: 510(k) (Traditional)
- Applicant: Fertipro NV
- Decided: Aug 16, 2007 after 212 days
- Product code: MQL (Media, Reproductive)
- Device class: 2
- Regulation: 21 CFR 884.6180
- 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 K060168 (2006). 1 ancestor in all.
1 later device descends from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K060168: Vitrification Freeze Kit, Vitrification Thaw Kit, Irvine Scientific Sales Co., Inc. (2006) Summary page 1.

## Most influential descendants
- K092107: Vitriblast, Thermoblast, Model VB-010, TB-010 (2010), 0 descendants of its own

## Indications for use
VitriFreeze Media are intended for ultra-rapid freezing of human blastocysts for Assisted Reproductive Technology (A.R.T.) procedures. VitriThaw media are intended for the recovery of human blastocysts that have undergone ultra-rapid freezing for Assisted Reproductive Technology (A.R.T.) procedures.

Source page: https://510kreport.com/device/K070135
Methodology: https://510kreport.com/methodology