510(k) Report

FDA applicant

Scott Paper Co.

Philadelphia, PA3 decisions1993–19930 recalls

FDA records 3 decisions for Scott Paper Co. (Philadelphia, PA) in 1993: 3 510(k) clearances. All are in product code HHD (Pad, Menstrual, Unscented). No recall is linked to its devices.

FDA’s records also spell it “Scott Paper , Ltd.”.

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 Scott Paper Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Scott Paper Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Scott”

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