# K002805: Kendro Heracell CO2 Incubator

- Pathway: 510(k) (Traditional)
- Applicant: Kendro Laboratory Products, L.P.
- Decided: Nov 9, 2000 after 62 days
- Product code: MQG (Accessory, Assisted Reproduction)
- Device class: 2
- Regulation: 21 CFR 884.6120
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
3 later devices descend from it; 3 cite it directly.
0 of 4 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
- K023465: Kendro Heracell 240 Incubator (2003), 1 descendant of its own
- K101988: Heal Force CO2 Incubator (2011), 0 descendants of its own
- K013703: Sanyo CO2 Incubators, Models Nos. Mco-17AC, Mco-17AIC, Mco-20AIC,and MC0-175M (2001), 0 descendants of its own

Source page: https://510kreport.com/device/K002805
Methodology: https://510kreport.com/methodology