# K070047: Nunc Ivf Dishes and Nunc Ivf 4-Well Dish

- Pathway: 510(k) (Traditional)
- Applicant: Nunc A/S
- Decided: May 18, 2007 after 134 days
- Product code: MQK (Labware, Assisted Reproduction)
- Device class: 2
- Regulation: 21 CFR 884.6160
- 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 K040717 (2004). 1 ancestor in all.
12 later devices descend from it; 1 cites it directly.
0 of 14 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K040717: Nunc Ivf Multidish 4 Wells Nunclon, Nunc A/S (2004) Summary page 1.

## Most influential descendants
- K092183: Embryoscope and Embryoslide (2011), 11 descendants of its own
- K111715: Embryoscope (2011), 9 descendants of its own
- K113075: Embryo Viewer Software (2011), 8 descendants of its own
- K150961: EmbryoSlide Culture Dish (2015), 4 descendants of its own
- K133712: Embryoviewer Software (2014), 4 descendants of its own

## Indications for use
Nunc IVF 4-Well Dishes are intended for preparing, storing, manipulation or transferring human gametes or embryos for in-vitro fertilization (IVF), or other in vitro fertilization techniques and cell culture. Nunc IVF PetriDishes are intended for preparing, storing, manipulation or transferring human gametes or embryos for in-vitro fertilization (IVF), or other in vitro fertilization techniques and cell culture.

Source page: https://510kreport.com/device/K070047
Methodology: https://510kreport.com/methodology