# K202490: Avid CT2

- Pathway: 510(k) (Traditional)
- Applicant: Vision Quest Industries Inc./Dba VQ Orthocare
- Decided: Nov 16, 2020 after 77 days
- Product code: IPF (Stimulator, Muscle, Powered)
- Device class: 2
- Regulation: 21 CFR 890.5850
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 4 generations back to K931781 (1993). 11 ancestors in all.
No later device cites it as a predicate yet.
0 of 12 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K982388: Surgi Stim, Vision Quest Industries, Inc. (1998) Summary page 4.
- K183692: Avid IF2, Vision Quest Industries Inc./Dba VQ Orthocare (2019) Summary page 4.

## Indications for use
Interferential Stimulation can be used in the following applications: • Symptomatic relief of post-surgical and/or post traumatic acute pain • Symptomatic relief of chronic intractable pain • Relaxation of muscle spasms • Maintain or increase range of motion • Increase local blood circulation Neuromuscular Stimulation can be used in the following applications: • Immediate postsurgical stimulation of calf muscles to prevent venous thrombosis • Prevention or retardation of disuse atrophy • Muscle-re-education

Source page: https://510kreport.com/device/K202490
Methodology: https://510kreport.com/methodology