# K915159: Pediatric Multi-Function Electrodes

- Pathway: 510(k) (Traditional)
- Applicant: Zmi Corp.
- Decided: Feb 7, 1992 after 85 days
- Product code: DRF (Catheter, Electrode Recording, Or Probe, Electrode Recording)
- Device class: 2
- Regulation: 21 CFR 870.1220
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 2 cite it directly.
0 of 3 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
- K072430: Zoll Pedipadz Reduced Energy Electrode (2007), 0 descendants of its own
- K040256: Pedi-Padz Radiolucent Multi-Function Pediatric Electrodes, Model 8900-1005 (2004), 0 descendants of its own

## Recalls of this device
- Jul 30, 2004 · Not classified · Z-1380-04: Pads may fail due to excessive corrosion of the electrode prior to the expiration date

Source page: https://510kreport.com/device/K915159
Methodology: https://510kreport.com/methodology