510(k) Report

510(k) · Cleared

Cleared

Licemeister Comb

K981250510(k) TraditionalCleared May 28, 199852-day reviewClass I21 CFR 880.5960

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

National Pediculosis Assoc. · LJL Detectors And Removers, Lice, (Including Combs)

Cleared on May 28, 1998 after a 52-day review. FDA’s file for it is a 510(k) statement, which names no predicate. 1 later device descends from it.

Decided
May 28, 1998
Review
52 days
Class
Class I
Product code
LJL
Recalls
None
Predicates
0

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

Descendants, by year cleared 1999: 1 descendant cleared1995200020052010201520202025
  1. This deviceK981250 Licemeister CombNational Pediculosis Assoc. · 1998
  2. Descendant · cites it directly · 0 of its ownK991958 Klout Shampoo and Lice Combing Pretreatment KitKiel Laboratories, Inc. · 1999

Most influential descendants

Showing 1 of 1 · See all
  • K991958Klout Shampoo and Lice Combing Pretreatment KitKiel Laboratories, Inc. · 1999 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K981250Licemeister CombNational Pediculosis Assoc.1998—
+1K991958Klout Shampoo and Lice Combing Pretreatment KitKiel Laboratories, Inc.1999—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
199910
FIG. 1 — Lineage of K981250, 1998–1999Source: 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), the FDA 510(k) statement (indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in LJL? 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’s file for it is a 510(k) statement, which names no predicate.

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K991958Klout Shampoo and Lice Combing Pretreatment KitKiel Laboratories, Inc.19990

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, K991958 (Kiel Laboratories, Inc., 1999) has gone furthest, with 0 descendants of its own.

How does its category compare?

All LJL devices

LJL Detectors And Removers, Lice, (Including Combs): FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · LJL

2in 2017

2009: 22017: 2
2007high 2 (2009) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · LJL

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

Recalls per year · LJL

No recall names LJL since 2007.

Adverse event reports per year · LJL

2in 2024

2018: 12020: 12023: 12024: 2
2007high 2 (2024) · low 0 (2007)2025

MAUDE reports naming product code LJL, 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
20092—00
20100—00
20110—00
20120—00
20130—00
20140—00
20150—00
20160—00
20172—00
20180—01
20190—00
20200—01
20210—00
20220—00
20230—01
20240—02
20250—00
20260—0—

What is it indicated for?

Combines screening & early detection of individual lice & their eggs

Indications for use read by OCR from a scanned FDA 510(k) statement, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K981250: Licemeister Comb.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K981250

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
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026