510(k) · Cleared

Cleared

Legacy-500

K111588510(k) TraditionalCleared Oct 26, 2012507-day reviewClass II21 CFR 890.5880

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Mt Tables, LLC · JFB Table, Physical Therapy, Multi Function

Cleared on Oct 26, 2012 as substantially equivalent to K010252 (Magnum Equipment LLC, 2001) and 2 other predicates after a 507-day review. Its family tree reaches back 2 generations to 2000.

Decided: Oct 26, 2012
Review: 507 days
Class: Class II
Product code: JFB
Recalls: None
Predicates: 3

Its longest line of descent runs back 2 generations to K993461 (2000). 3 ancestors in all. No later device cites it as a predicate yet.

By dateBy generation

Root · 2 generations backK993461 Quest Intersegmental Roller Traction TableIcon Intl., LLC · 2000
1 generation backK002390 Quantum Intersegmental Traction Table 400, 401, 400H,401HLsi Intl., Inc. · 2000
This deviceK111588 Legacy-500Mt Tables, LLC · 2012

View FIG. 1 as a table

Line of descent and top descendants

Generation	Number	Device	Applicant	Decided	Recalls
−2	K993461	Quest Intersegmental Roller Traction Table	Icon Intl., LLC	2000	—
−1	K002390	Quantum Intersegmental Traction Table 400, 401, 400H,401H	Lsi Intl., Inc.	2000	—
0 (this device)	K111588	Legacy-500	Mt Tables, LLC	2012	—

Other ancestors by year cleared

Year cleared	Devices	With a Class I recall
2001	1	0

FIG. 1 — Lineage of K111588, 2000–2012Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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 JFB? 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 JFB device

#1 K240168 N7-Sscore 9.8 · 7 generations · no Class I recall
#2 Held for the reportin the report
#3 Held for the reportin the report

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What was it cleared against? (3)

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	Applicant	Decided	Recalls
*	K010252	Magnum Summary page 1 …CFR 890.5880 Regulatory Class: Class 11 Product Code: JFB Part 890- : SEC. 890.5880 Multi-Function Physical Therapy Table Substantial K010252 Magnum, K(002390 Quantum 400, K(993461 Quest 1ST Equivalence: Device Description: Legacy-SOD Massage Table isan electrically pow…	Magnum Equipment LLC	2001	—
*	K002390	Quantum Intersegmental Traction Table 400, 401, 400H,401H Summary page 1 …ulatory Class: Class 11 Product Code: JFB Part 890- : SEC. 890.5880 Multi-Function Physical Therapy Table Substantial K010252 Magnum, K(002390 Quantum 400, K(993461 Quest 1ST Equivalence: Device Description: Legacy-SOD Massage Table isan electrically powered, motorized,…	Lsi Intl., Inc.	2000	—
*	K993461	Quest Intersegmental Roller Traction Table Summary page 1 …ss 11 Product Code: JFB Part 890- : SEC. 890.5880 Multi-Function Physical Therapy Table Substantial K010252 Magnum, K(002390 Quantum 400, K(993461 Quest 1ST Equivalence: Device Description: Legacy-SOD Massage Table isan electrically powered, motorized, multifunctional physic…	Icon Intl., LLC	2000	—

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 12 years and passes through 3 companies; a new generation was cleared every 12.0 years on median.
None of the 3 ancestors has a recall.

How does its category compare?

All JFB devices

JFB Table, Physical Therapy, Multi Function: FDA decisions, review times, recalls and adverse event reports over 20 years. 2012, this device’s year, is highlighted.

FDA decisions per year · JFB

3in 2025

2007high 3 (2025) · low 0 (2009)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · JFB

162in 2025

2007high 162 (2025)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · JFB

No recall names JFB since 2007.

Adverse event reports per year · JFB

1in 2024

2007high 3 (2007) · low 0 (2014)2025

MAUDE reports naming product code JFB, not matched to any one device; reports are not rates.

View these four charts as a table

Year	Decisions	Median 510(k) review, days	MAUDE reports
2007	1	—	3
2008	1	—	3
2009	0	—	3
2010	2	—	1
2011	2	—	1
2012	2	—	2
2013	0	—	2
2014	1	—	0
2015	0	—	0
2016	1	—	0
2017	0	—	0
2018	0	—	0
2019	0	—	0
2020	0	—	1
2021	2	—	0
2022	1	—	2
2023	0	—	0
2024	2	—	1
2025	3	162	0
2026	0	—	—

What is it indicated for?

The intended use is to provide muscle relaxation therapy by delivering a soothing massage.

Indications for use as stated in the FDA summary.

https://510kreport.com/device/K111588 · printed Nov 6, 2026

Cite this page

510(k) Report. “K111588: Legacy-500.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K111588

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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