510(k) Report

510(k) · Cleared

Cleared

Auto Therm 390, Model ME 390

K042554510(k) AbbreviatedCleared Oct 8, 200418-day reviewClass II21 CFR 890.5290

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

Mettler Electronics Corp. · IMJ Diathermy, Shortwave, For Use In Applying Therapeutic Deep Heat

Cleared on Oct 8, 2004 after an 18-day review. The FDA summary names its predicate without a number. 63 later devices descend from it.

Decided
Oct 8, 2004
Review
18 days
Class
Class II
Product code
IMJ
Recalls
None
Predicates
0

63 later devices descend from it, 3 citing it directly.

Descendants, by year cleared 2009: 2 descendants cleared2016: 9 descendants cleared2014: 4 descendants cleared2012: 1 descendant cleared2017: 4 descendants cleared2015: 2 descendants cleared2013: 1 descendant cleared2019: 6 descendants cleared2022: 5 descendants cleared2021: 4 descendants cleared2020: 4 descendants cleared2026: 5 descendants cleared2018: 1 descendant cleared2025: 8 descendants cleared2024: 4 descendants cleared2023: 3 descendants cleared200020052010201520202025
  1. This deviceK042554 Auto Therm 390, Model ME 390Mettler Electronics Corp. · 2004
  2. Descendant · cites it directly · 61 of its ownK083433 Intelect SWD 100, Model 1600; Senior Solutions Shortwave Diathermy…Chattanooga Group · 2009 · Recalled
  3. Descendant · cites it directly · 54 of its ownK090221 Reaction SystemViora, Ltd. · 2009
  4. Descendant · 2 generations on · 33 of its ownK133837 Viora V-TotalViora, Ltd. · 2014
  5. Descendant · 3 generations on · 32 of its ownK142093 V20 SystemViora, Ltd. · 2014
  6. Descendant · 2 generations on · 31 of its ownK150035 V10 systemViora, Ltd. · 2015

Showing 5 of 63 descendants. See all descendants

Descendants cleared per year

2009: 22012: 12013: 12014: 42015: 22016: 92017: 42018: 12019: 62020: 42021: 42022: 52023: 32024: 42025: 82026: 5
2009high 9 (2016) · low 0 (2010)2026

Most influential descendants

Showing 5 of 63 · See all
  • K083433Intelect SWD 100, Model 1600; Senior Solutions Shortwave Diathermy, Model 1601Chattanooga Group · 2009 · cites it directly61descendants
  • K090221Reaction SystemViora, Ltd. · 2009 · cites it directly54descendants
  • K133837Viora V-TotalViora, Ltd. · 2014 · 2 generations on33descendants
  • K142093V20 SystemViora, Ltd. · 2014 · 3 generations on32descendants
  • K150035V10 systemViora, Ltd. · 2015 · 2 generations on31descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K042554Auto Therm 390, Model ME 390Mettler Electronics Corp.2004—
+1K083433Intelect SWD 100, Model 1600; Senior Solutions Shortwave Diathermy, Model 1601Chattanooga Group20091
+1K090221Reaction SystemViora, Ltd.2009—
+2K133837Viora V-TotalViora, Ltd.2014—
+3K142093V20 SystemViora, Ltd.2014—
+2K150035V10 systemViora, Ltd.2015—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200920
201210
201310
201440
201520
201690
201740
201810
201960
202040
202140
202250
202330
202440
202580
202650
FIG. 1 — Lineage of K042554, 2004–2026Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

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 IMJ? 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 IMJ device

  1. #1 K252963 BTL-899TTscore 12.4 · 4 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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What was it cleared against? (1)

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.

TypeNumberDeviceApplicantDecidedRecalls
*—Auto*Therm 395, Model 395
Named without a submission number
—

What descends from it? (63)

See all 63

3 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K083433Intelect SWD 100, Model 1600; Senior Solutions Shortwave Diathermy, Model 1601Chattanooga Group200961
K090221Reaction SystemViora, Ltd.200954
K162240ProMedTek Model C1400 Shortwave Diathermy DevicePromedtek, Inc.20160

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?

  • Of its descendants, K083433 (Chattanooga Group, 2009) has gone furthest, with 61 descendants of its own.

How does its category compare?

All IMJ devices

IMJ Diathermy, Shortwave, For Use In Applying Therapeutic Deep Heat: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · IMJ

2in 2025

2009: 12012: 12014: 32016: 32018: 12019: 12023: 12025: 22026 (partial year): 1
2007high 3 (2014) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · IMJ

131in 2016

2014: 393 days median2016: 131 days median
2007high 393 (2014) · low 131 (2016)2026

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

Recalls per year · IMJ

1in 2015

2015: 1
2007high 1 (2015) · low 0 (2007)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · IMJ

1in 2019

2009: 12010: 12011: 32012: 22013: 42014: 32015: 52017: 22019: 1
2007high 5 (2015) · low 0 (2007)2025

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

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20070—00
20080—00
20091—01
20100—01
20110—03
20121—02
20130—04
2014339303
20150—15
2016313100
20170—02
20181—00
20191—01
20200—00
20210—00
20220—00
20231—00
20240—00
20252—00
20261—0—

What is it indicated for?

Shortwave diathermy delivers energy in the radio band of 27.12 MHz to provide deep heating therapeutic effects to body tissues. When shortwave diathermy is delivered to the body at intensities capable of generating a deep tissue temperature increase, it can be used to treat selected medical conditions such as:

1. Relieving pain

2. Reducing muscle spasm

3. Increasing range of motion of contracted joints using heat and stretch techniques.

4. Increasing blood flow to tissues in the treatment area.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K042554: Auto Therm 390, Model ME 390.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K042554

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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