# K042105: Clipper Diagnostic Electrode Catheter

- Pathway: 510(k) (Special)
- Applicant: Bard Electrophysiology
- Decided: Sep 23, 2004 after 50 days
- Product code: DRF (Catheter, Electrode Recording, Or Probe, Electrode Recording)
- Device class: 2
- Regulation: 21 CFR 870.1220
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Bard Viking Diagnostic Electrode Catheter: named in the summary without a submission number
- (no number) Bard Woven Diagnostic Electrode Catheter: named in the summary without a submission number

## Indications for use
Bard Electrophysiology's fixed diagnostic electrode catheters are intended for temporary intracardiac sensing, recording, stimulation and temporary pacing during the evaluation of cardiac arrhythmias.

Source page: https://510kreport.com/device/K042105
Methodology: https://510kreport.com/methodology