# K933649: Conmed Ecg Patient Cables and Leadwires

- Pathway: 510(k) (Traditional)
- Applicant: Conmedcorp
- Decided: Feb 18, 1994 after 206 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.
11 later devices descend from it; 2 cite it directly.
0 of 12 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
- K980582: Multi-Link Cable and Lead Wire Systems (1998), 10 descendants of its own
- K082851: Multlink Cable and Leadwire System (2008), 7 descendants of its own
- K101660: Ecg Single Patient Use Lead Wire Set, Models 2048801-5 to 2048801-8 (2010), 6 descendants of its own
- K162432: Multi-Link X2 ECG Cable and Lead Wire System (2017), 3 descendants of its own
- K211294: Multi-Link X2 ECG Cable and Leadwire System (2021), 1 descendant of its own

Source page: https://510kreport.com/device/K933649
Methodology: https://510kreport.com/methodology