FDA applicant

Amsco American Sterilizer Co.

Erie, PA1 decision1994–19940 recalls

FDA records 1 decision for Amsco American Sterilizer Co. (Erie, PA) in 1994: 1 510(k) clearance. All are in product code FWW (Table, Operating-Room, Pneumatic). 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 and plastic surgery panel, where it files most

How often FDA has decided Amsco American Sterilizer Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Amsco American Sterilizer Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Amsco American Sterilizer Co.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Amsco”

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

Amsco Co. 19 Amsco Sterile Recoveries, Inc. 12 Amsco Hospital Products Co. 1 Amsco Intl., Inc. 1

Amsco American Sterilizer Co.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Amsco”