# K945034: Conmed Ecg Patient Safety Cables and Leadwires-Removal and Permanently-Attached Leadwires

- Pathway: 510(k) (Traditional)
- Applicant: Conmedcorp
- Decided: Oct 27, 1994 after 14 days
- Product code: DSA (Cable, Transducer And Electrode, Patient, (Including Connector))
- Device class: 2
- Regulation: 21 CFR 870.2900
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K070232: Ecg Cables, Trunk and Patient Lead Wires (2007), 0 descendants of its own

Source page: https://510kreport.com/device/K945034
Methodology: https://510kreport.com/methodology