# K081279: Pro-Tech Delivery System Electrodes, Model TT-2000

- Pathway: 510(k) (Traditional)
- Applicant: Transfer Technology
- Decided: Jan 23, 2009 after 262 days
- Product code: GXY (Electrode, Cutaneous)
- Device class: 2
- Regulation: 21 CFR 882.1320
- 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 K875284 (1988). 3 ancestors in all.
No later device cites it as a predicate yet.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K000870: KM-10 Tens Electrode, Katecho, Inc. (2000) Summary page 1.
- K970426: Valuetrode, Axelgaard Mfg. Co., Ltd. (1997) Summary page 1.
- K875284: Medtronic Snap Ease Model 7795 Cutaneous Electrode, Medtronic Vascular (1988) Summary page 1.

## Indications for use
The Transfer Technology PRO-TECH Delivery System electrodes are intended for use as a disposable, conductive adhesive interface between the patient's skin and the Electrical Stimulator Transfer Technology's reusable electrodes are designed and intended to be used with marketed, Electrical Stimulators, ie TENS (Transcutaneous Electrical Nerve Stimulation), EMS (Electrical Muscular Stimulation), and MANS (Muscle and Neurological Stimulators)

Source page: https://510kreport.com/device/K081279
Methodology: https://510kreport.com/methodology