# K851097: Lode Model Corival Ergometer

- Pathway: 510(k) (Traditional)
- Applicant: Lode Corp.
- Decided: Jun 18, 1985 after 91 days
- Product code: ISD (Exerciser, Measuring)
- Device class: 2
- Regulation: 21 CFR 890.5360
- 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; 2 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
- K053078: Ergoselect 100 K/P, Ergoselect 200 K/P (2006), 1 descendant of its own
- K112121: Ergoselect/GE (2012), 0 descendants of its own
- K990813: Rehcor (1999), 0 descendants of its own

Source page: https://510kreport.com/device/K851097
Methodology: https://510kreport.com/methodology