# K953737: VL7600 Rem Patient Return Electrode

- Pathway: 510(k) (Traditional)
- Applicant: Valleylab, Inc.
- Decided: Aug 23, 1995 after 13 days
- Product code: GEI (Electrosurgical, Cutting & Coagulation & Accessories)
- Device class: 2
- Regulation: 21 CFR 878.4400
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
12 later devices descend from it; 1 cites it directly.
3 of 13 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K994428: E7512 Premie Rem Polyhesive II Patient Return Electrode (2000), 11 descendants of its own
- K140500: Skintact (2014), 4 descendants of its own
- K080741: Mega Soft Reusable Patient Return Electrode (2008), 4 descendants of its own
- K173877: BOWA Neutral Electrodes (2018), 3 descendants of its own
- K133726: Mega Soft Universal Patient Return Electrode (2014), 3 descendants of its own

Source page: https://510kreport.com/device/K953737
Methodology: https://510kreport.com/methodology