# K081762: Curbell Patient Monitoring Cables

- Pathway: 510(k) (Abbreviated)
- Applicant: Curbell Electronics, Inc.
- Decided: Aug 27, 2008 after 68 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
Longest line of descent: 1 generation back to K942321 (1994). 1 ancestor in all.
3 later devices descend from it; 2 cite it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K942321: Variouspatient Monitoring Cable, Merit Cables Incorporated (1994) Summary page 1.

## Most influential descendants
- K181726: Medline Patient Cables and Lead Wires (2018), 1 descendant of its own
- K243545: Philips Reusable ECG Lead Sets and Trunk Cables : Model Number,Model Name: 989803170171, OR 3-Lead ECG Trunk Cable, AAMI/IEC;  989803170181, OR 5-Lead ECG Trunk Cable, AAMI/IEC;  M1667A, 6 Lead ECG Trunk, AAMI/IEC 2.7m;  M1668A,5 Lead ECG Trunk, AAMI/IEC 2.7m;  M1669A,3 Lead ECG Trunk, AAMI/IEC 2.7m;  M1949A,5+5 ECG Trunk cable AAMI, IEC 2.7m;  M1663A,10 Lead ECG Trunk AAMI/IEC 2m;  M1665A, 6+4 Lead ECG Trunk AAMI/IEC 2.7m;  M1671A, 3 Leadset, Grabber, AAMI, ICU;  M1673A, 3 Leadset, Sn (2025), 0 descendants of its own
- K182220: Curbell branded Patient Monitoring Cables (2018), 0 descendants of its own

## Indications for use
Curbell patient cables are used to connect electrodes and/or sensors placed at the appropriate sites on the patient to a monitoring device for general monitoring and/or diagnostic evaluation by a healthcare professional.

Source page: https://510kreport.com/device/K081762
Methodology: https://510kreport.com/methodology