# K083202: Combocare 2000

- Pathway: 510(k) (Traditional)
- Applicant: Xanacare Technologies, LLC
- Decided: Dec 15, 2008 after 46 days
- Product code: GZJ (Stimulator, Nerve, Transcutaneous, For Pain Relief)
- Device class: 2
- Regulation: 21 CFR 882.5890
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 6 generations back to K001179 (2000). 17 ancestors in all.
2 later devices descend from it; 2 cite it directly.
0 of 20 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K081141: Combocare 2000, Xanacare Technologies, LLC (2008) Summary page 1.
- K071445: Terraquant MQ2000 V.5 with the TQ-1TENS, Escada International, Inc. (2007) Summary page 1.

## Most influential descendants
- K160246: SimulCare II (TM) (2016), 0 descendants of its own
- K102278: Quadra Bloc Tens Plus (2011), 0 descendants of its own

## Indications for use
The ComboCare 2000 is intended for the temporary relief of minor muscle and joint pain, promoting the relaxation of muscle tissue, temporarily increasing local blood circulation, symptomatic relief and management of chronic intractable pain, and adjunctive relief of post-surgical or post-traumatic acute pain.

Source page: https://510kreport.com/device/K083202
Methodology: https://510kreport.com/methodology