510(k) Report

FDA applicant

Care Technologies, Inc.

Washington, DC2 decisions1998–19980 recalls

FDA records 2 decisions for Care Technologies, Inc. (Washington, DC) in 1998: 2 510(k) clearances. All are in product code LJL (Detectors And Removers, Lice, (Including Combs)). Its devices cite 4 predicates, 0 of them its own earlier devices. 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 Care Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Care Technologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Care Technologies, Inc. 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)2decisions

Whose devices does it build on?

Its devices cite 4 predicates; 0 are its own earlier devices. The firms it cites most:

Who builds on its devices?

Later devices cite its devices 2 times; 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.

  • K981147Clear (TM) Lice Egg Remover SystemCare Technologies, Inc. · 19982cite it

What has FDA decided for it lately?

  • K981147Clear (TM) Lice Egg Remover SystemCare Technologies, Inc. · 1998
  • K981037Clear (TM) Special Nit CombCare Technologies, Inc. · 1998

All 2 as Care Technologies, Inc. →