FDA applicant

Hudson Extrusions, Inc.

Hudson, OH2 decisions1984–19840 recalls

FDA records 2 decisions for Hudson Extrusions, Inc. (Hudson, OH) in 1984: 2 510(k) clearances. All are in product code CAT (Cannula, Nasal, Oxygen). 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, anesthesiology panel, where it files most

How often FDA has decided Hudson Extrusions, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Hudson Extrusions, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Hudson Extrusions, Inc.’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 “Hudson”

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

Hudson Oxygen Therapy Sales Co. 33 Hudson Respiratory Care, Inc. 15 Hudson Diagnostic Imaging, LLC 2 Hudson Kendale Assoc., Inc. 1 Hudson Rcj AB 1

Hudson Extrusions, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Hudson”