# K896396: Mida System, Models 1000/1100

- Pathway: 510(k) (Traditional)
- Applicant: Medical Graphics Corp.
- Decided: Jan 18, 1990 after 73 days
- Product code: DYC (Vectorcardiograph)
- Device class: 2
- Regulation: 21 CFR 870.2400
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
5 later devices descend from it; 2 cite it directly.
0 of 6 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
- K042002: Synescope, Easyscope, Synecom, Holterreader (2004), 3 descendants of its own
- K193177: CER-S (2020), 2 descendants of its own
- K213861: CER-S (2022), 1 descendant of its own
- K243312: CER-S (2025), 0 descendants of its own
- K023414: Mida Algorithm Rev. B (2003), 0 descendants of its own

Source page: https://510kreport.com/device/K896396
Methodology: https://510kreport.com/methodology