510(k) Report

FDA applicant

Anderson Winn Paper Co.

Burbank, CA2 decisions1989–19930 recalls

FDA records 2 decisions for Anderson Winn Paper Co. (Burbank, CA) from 1989 to 1993: 2 510(k) clearances. All are in product code HHT (Spatula, Cervical, Cytological). 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, obstetrics and gynecology panel, where it files most

How often FDA has decided Anderson Winn Paper Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Anderson Winn Paper Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Anderson Winn Paper Co. 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?

  • HHTSpatula, Cervical, Cytological2decisions

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.

  • K924908Cell Collecting BrushAnderson Winn Paper Co. · 19931cites it

What has FDA decided for it lately?

  • K924908Cell Collecting BrushAnderson Winn Paper Co. · 1993
  • K890283Cytex One and Cytex TwoAnderson Winn Paper Co. · 1989

All 2 as Anderson Winn Paper Co. →

Other applicant names beginning “Anderson”

FDA records each applicant name separately; these may or may not be the same firm.

Anderson Research, Inc. 1