510(k) Report

FDA applicant

National Pediculosis Assoc.

Needham, MA1 decision1998–19980 recalls

FDA records 1 decision for National Pediculosis Assoc. (Needham, MA) in 1998: 1 510(k) clearance. All are in product code LJL (Detectors And Removers, Lice, (Including Combs)). No recall is linked to its devices.

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

FIG. A — Illustration, general hospital panel, where it files most

How often FDA has decided National Pediculosis Assoc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for National Pediculosis Assoc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — National Pediculosis Assoc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • LJLDetectors And Removers, Lice, (Including Combs)1decision

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K981250Licemeister CombNational Pediculosis Assoc. · 19981cites it

What has FDA decided for it lately?

  • K981250Licemeister CombNational Pediculosis Assoc. · 1998

The one decision as National Pediculosis Assoc. →