510(k) Report

FDA applicant

Cl Mcintosh

Rockville, MD1 decision2002–20020 recalls

FDA records 1 decision for Cl Mcintosh (Rockville, MD) in 2002: 1 510(k) clearance. All are in product code LPL (Lenses, Soft Contact, Daily Wear). 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, ophthalmic panel, where it files most

How often FDA has decided Cl Mcintosh’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Cl Mcintosh since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Cl Mcintosh 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?

  • LPLLenses, Soft Contact, Daily Wear1decision

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.

  • K020193Ocular Sciences, Inc. Biomedics UV Asphere (Ocufilcon D) Soft (Hydrophilic) Contact LensCl Mcintosh · 20022cite it

What has FDA decided for it lately?

  • K020193Ocular Sciences, Inc. Biomedics UV Asphere (Ocufilcon D) Soft (Hydrophilic) Contact LensCl Mcintosh · 2002

The one decision as Cl Mcintosh →