510(k) · Cleared
ClearedAvid CT2
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Vision Quest Industries Inc./Dba VQ Orthocare · IPF Stimulator, Muscle, Powered
Cleared on Nov 16, 2020 as substantially equivalent to K982388 (Vision Quest Industries, Inc., 1998) and 1 other predicate after a 77-day review. Its family tree reaches back 4 generations to 1993.
- Decided
- Nov 16, 2020
- Review
- 77 days
- Class
- Class II
- Product code
- IPF
- Recalls
- None
- Predicates
- 2
Its longest line of descent runs back 4 generations to K931781 (1993). 11 ancestors in all, the oldest K872976 (1987). No later device cites it as a predicate yet.
- Root · 4 generations backK931781 Jace Tri-Stim DeviceJace Systems, Inc. · 1993
- 3 generations backK030507 T.E.a.R. TECH3 Model #44TT03Vision Quest Industries, Inc. · 2003
- 2 generations backK090532 T.E.a.R. TECH3Vision Quest Industries, Inc. · 2009
- 1 generation backK183692 Avid IF2Vision Quest Industries Inc./Dba VQ Orthocare · 2019
- This deviceK202490 Avid CT2Vision Quest Industries Inc./Dba VQ Orthocare · 2020
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −4 | K931781 | Jace Tri-Stim Device | Jace Systems, Inc. | 1993 | — |
| −3 | K030507 | T.E.a.R. TECH3 Model #44TT03 | Vision Quest Industries, Inc. | 2003 | — |
| −2 | K090532 | T.E.a.R. TECH3 | Vision Quest Industries, Inc. | 2009 | — |
| −1 | K183692 | Avid IF2 | Vision Quest Industries Inc./Dba VQ Orthocare | 2019 | — |
| 0 (this device) | K202490 | Avid CT2 | Vision Quest Industries Inc./Dba VQ Orthocare | 2020 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1987 | 1 | 0 |
| 1992 | 2 | 0 |
| 1993 | 1 | 0 |
| 1997 | 1 | 0 |
| 1998 | 1 | 0 |
| 2005 | 1 | 0 |
Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.
Planning a device in IPF? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.
Top candidate predicates for a new IPF device
- #1 K241433 EVE Synergy (EVE-20M)score 19.6 · 25 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (2)
Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K982388 | Surgi StimSummary page 4…21CFR 890.5850, Product Code IPF Predicate Devices: Surgi Stim/T.E.A.R. Tech by Vision Quest Industries, Inc. K982388 and Avid IF2 by Vision Quest Industries, Inc.K183692 Device Description: The Avi… | 1998 |
| * | K183692 | Avid IF2Summary page 4…m/T.E.A.R. Tech by Vision Quest Industries, Inc. K982388 and Avid IF2 by Vision Quest Industries, Inc.K183692 Device Description: The Avid CT2, Model AV-CT20A is a combination therapy device… | 2019 |
What descends from it?
No later submission names this one as a predicate yet.
Has anything in its family been recalled? (0 Class I)
No FDA recall names this device.
No ancestor or descendant has a Class I recall.
What does this lineage say?
- The line of descent spans 27 years and passes through 3 companies; a new generation was cleared every 9.6 years on median.
- None of the 11 ancestors has a recall.
- 1 other device also cites its predicate K982388.
How does its category compare?
All IPF devicesIPF Stimulator, Muscle, Powered: FDA decisions, review times, recalls and adverse event reports over 20 years. 2020, this device’s year, is highlighted.
FDA decisions per year · IPF
3in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · IPF
257in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · IPF
1in 2023
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · IPF
8in 2025
MAUDE reports naming product code IPF, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 8 | 143 | 0 | 11 |
| 2008 | 6 | 140 | 1 | 213 |
| 2009 | 7 | 216 | 0 | 150 |
| 2010 | 4 | 121 | 0 | 14 |
| 2011 | 4 | 275 | 1 | 25 |
| 2012 | 4 | 269 | 3 | 16 |
| 2013 | 10 | 180 | 0 | 6 |
| 2014 | 4 | 264 | 0 | 19 |
| 2015 | 3 | 43 | 0 | 11 |
| 2016 | 7 | 113 | 0 | 8 |
| 2017 | 5 | 110 | 0 | 2 |
| 2018 | 5 | 73 | 0 | 3 |
| 2019 | 4 | 133 | 0 | 10 |
| 2020 | 9 | 121 | 0 | 13 |
| 2021 | 15 | 98 | 0 | 3 |
| 2022 | 7 | 108 | 0 | 4 |
| 2023 | 9 | 255 | 1 | 8 |
| 2024 | 7 | 201 | 0 | 5 |
| 2025 | 3 | 257 | 0 | 8 |
| 2026 | 3 | 206 | 0 | — |
What is it indicated for?
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
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K202490 · printed Nov 6, 2026
Cite this page
510(k) Report. “K202490: Avid CT2.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K202490
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Record history
- FDA decision record loaded May 2, 2026
- Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
- Lineage and recalls computed Nov 3, 2026
- Page last updated Nov 3, 2026