510(k) Report

510(k) · Cleared

Cleared

CW-Disposable Acupuncture Needle

K962419510(k) TraditionalCleared Jul 25, 199631-day reviewClass II21 CFR 880.5580

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

Acupuncture Supplies Import Co. · MQX Needle, Acupuncture, Single Use

Cleared on Jul 25, 1996 after a 31-day review. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known. 2 later devices descend from it.

Decided
Jul 25, 1996
Review
31 days
Class
Class II
Product code
MQX
Recalls
None
Predicates
0

2 later devices descend from it, 2 citing it directly.

Descendants, by year cleared 1998: 2 descendants cleared1995200020052010201520202025
  1. This deviceK962419 CW-Disposable Acupuncture NeedleAcupuncture Supplies Import Co. · 1996
  2. Descendant · cites it directly · 0 of its ownK980470 KHT Soft Sooji Needle, Hand Acupuncture NeedleAmerican Institute of Koryo Hand Therapy · 1998
  3. Descendant · cites it directly · 0 of its ownK974527 KHT Seoam Needle, Hand Acupuncture NeedleAmerican Institute of Koryo Hand Therapy · 1998

Most influential descendants

Showing 2 of 2 · See all
  • K980470KHT Soft Sooji Needle, Hand Acupuncture NeedleAmerican Institute of Koryo Hand Therapy · 1998 · cites it directly0descendants
  • K974527KHT Seoam Needle, Hand Acupuncture NeedleAmerican Institute of Koryo Hand Therapy · 1998 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K962419CW-Disposable Acupuncture NeedleAcupuncture Supplies Import Co.1996—
+1K980470KHT Soft Sooji Needle, Hand Acupuncture NeedleAmerican Institute of Koryo Hand Therapy1998—
+1K974527KHT Seoam Needle, Hand Acupuncture NeedleAmerican Institute of Koryo Hand Therapy1998—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
199820
FIG. 1 — Lineage of K962419, 1996–1998Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Get the monthly Device Review Tracker

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 MQX? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

  • Candidate predicates for a device like this, rankedin the report
  • Recall history across each candidate’s familyin the report
Get a 510(k) Report

What was it cleared against?

FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

What descends from it? (2)

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

NumberDeviceApplicantDecidedDescendants
K980470KHT Soft Sooji Needle, Hand Acupuncture NeedleAmerican Institute of Koryo Hand Therapy19980
K974527KHT Seoam Needle, Hand Acupuncture NeedleAmerican Institute of Koryo Hand Therapy19980

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, K980470 (American Institute of Koryo Hand Therapy, 1998) has gone furthest, with 0 descendants of its own.

How does its category compare?

All MQX devices

MQX Needle, Acupuncture, Single Use: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · MQX

1in 2017

2007: 12008: 12009: 22010: 12011: 22013: 12014: 12015: 32017: 1
2007high 3 (2015) · low 0 (2012)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · MQX

245in 2015

2015: 245 days median
2007high 245 (2015)2026

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

Recalls per year · MQX

1in 2007

2007: 1
2007high 1 (2007) · low 0 (2008)2026

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

Adverse event reports per year · MQX

2in 2025

2008: 22013: 12014: 12015: 12016: 12018: 12023: 12024: 12025: 2
2007high 2 (2008) · low 0 (2007)2025

MAUDE reports naming product code MQX, 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
20071—10
20081—02
20092—00
20101—00
20112—00
20120—00
20131—01
20141—01
2015324501
20160—01
20171—00
20180—01
20190—00
20200—00
20210—00
20220—00
20230—01
20240—01
20250—02
20260—0—
Cite this page

510(k) Report. “K962419: CW-Disposable Acupuncture Needle.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K962419

Report an extraction error

Tell us what is wrong; we check it against the FDA summary.

Are you the manufacturer?

Send a correction or an update to this page, for example a newer model or a public statement about a recall.

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