510(k) Report

510(k) · Cleared

Cleared

BNS 40

K842224510(k) TraditionalCleared Nov 19, 1984167-day reviewClass II21 CFR 890.5850

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

Myo-Tronics Research, Inc. · NUW Stimulator, Muscle, Powered, Dental

Cleared on Nov 19, 1984 after a 167-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 1 later device descends from it.

Decided
Nov 19, 1984
Review
167 days
Class
Class II
Product code
NUW
Recalls
None
Predicates
0

1 later device descends from it, 1 citing it directly.

Descendants, by year cleared 2004: 1 descendant cleared19801990200020102020
  1. This deviceK842224 BNS 40Myo-Tronics Research, Inc. · 1984
  2. Descendant · cites it directly · 0 of its ownK040400 Myo-Trode SG Disposable ElectrodeMyotronics-Noromed, Inc. · 2004

Most influential descendants

Showing 1 of 1 · See all
  • K040400Myo-Trode SG Disposable ElectrodeMyotronics-Noromed, Inc. · 2004 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K842224BNS 40Myo-Tronics Research, Inc.1984—
+1K040400Myo-Trode SG Disposable ElectrodeMyotronics-Noromed, Inc.2004—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200410
FIG. 1 — Lineage of K842224, 1984–2004Source: 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), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in NUW? 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 NUW device

  1. #1 K243290 BTL-785MJscore 9.9 · 3 generations · no Class I recall
  2. #2 Held for the reportin the report
Get a 510(k) Report

What was it cleared against?

FDA has not posted a summary or statement for it, so its predicates are not known.

What descends from it? (1)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K040400Myo-Trode SG Disposable ElectrodeMyotronics-Noromed, Inc.20040

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, K040400 (Myotronics-Noromed, Inc., 2004) has gone furthest, with 0 descendants of its own.

How does its category compare?

All NUW devices

NUW Stimulator, Muscle, Powered, Dental: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · NUW

1in 2025

2021: 12025: 1
2007high 1 (2021) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · NUW

Too few NUW 510(k)s in any year since 2007 to give a median.

Recalls per year · NUW

No recall names NUW since 2007.

Adverse event reports per year · NUW

No MAUDE report names NUW since 2007.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20070—00
20080—00
20090—00
20100—00
20110—00
20120—00
20130—00
20140—00
20150—00
20160—00
20170—00
20180—00
20190—00
20200—00
20211—00
20220—00
20230—00
20240—00
20251—00
20260—0—
Cite this page

510(k) Report. “K842224: BNS 40.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K842224

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Record history
  • FDA decision record loaded May 2, 2026
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026