# K203556: Medtronic Model 5492A, 5492V, 5492AL, 5492VL Patient Cables

- Pathway: 510(k) (Traditional)
- Applicant: Medtronic, Inc.
- Decided: Jul 12, 2021 after 217 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 K960446 (1996). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K960446: Model 5471 & 5471L Sterile Disposable Patient Cable Assemblies, Medtronic Vascular (1996) Summary page 4.

## Indications for use
The Medtronic Model 5492A, 5492V, 5492AL, 5492VL patient cables are intended for use as part of a temporary cardiac pacing system. They connect atrial and ventricular pacing lead systems to a temporary external pacemaker. They are intended for use by trained clinicians in a clinical environment. For more information about the intended use of and the indications for temporary cardiac pacing systems, refer to the technical manuals for the cardiovascular stimulating instruments. The Model 5492A, 5492V, 5492AL, 5492VL reusable patient cables are intended to be used with: * Medtronic endocardial or myocardial pacing lead connector pins 0.38 to 2.41 mm (0.015 to 0.095 in.) in diameter and up to 25.4 mm (1.0 in.) long. * Medtronic cardiovascular stimulating instruments.

Source page: https://510kreport.com/device/K203556
Methodology: https://510kreport.com/methodology