510(k) Report

FDA applicant

North American Marketing Corp.

Santa Ynez, CA1 decision1991–19910 recalls

FDA records 1 decision for North American Marketing Corp. (Santa Ynez, CA) in 1991: 1 510(k) clearance. All are in product code OCT (Anti Fog Solution And Accessories, Endoscopy). 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, gastroenterology and urology panel, where it files most

How often FDA has decided North American Marketing Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for North American Marketing Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — North American Marketing Corp. 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?

  • OCTAnti Fog Solution And Accessories, Endoscopy1decision

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.

  • K904871Medi-KleerNorth American Marketing Corp. · 19911cites it

What has FDA decided for it lately?

  • K904871Medi-KleerNorth American Marketing Corp. · 1991

The one decision as North American Marketing Corp. →