# K061606: Defibrillator Cable Tester, Model DT2200

- Pathway: 510(k) (Traditional)
- Applicant: Medical Devices/Padpro, Inc.
- Decided: Jun 21, 2006 after 12 days
- Product code: DRG (Transmitters And Receivers, Physiological Signal, Radiofrequency)
- Device class: 2
- Regulation: 21 CFR 870.2910
- 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 K790394 (1979). 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)
- K790394: Defibrillator Interal Paddle Test Load, Physio-Control Corp. (1979) Summary page 1.

## Indications for use
This device is designed to serve as a 50 ohm cable test load for low energy DC defibrillators.

Source page: https://510kreport.com/device/K061606
Methodology: https://510kreport.com/methodology