FDA applicant

Ann Arbor Plastics, Inc.

Mchenry, IL2 decisions1979–19800 recalls

FDA records 2 decisions for Ann Arbor Plastics, Inc. (Mchenry, IL) from 1979 to 1980: 2 510(k) clearances. Most are in product codes FOG (Hood, Oxygen, Infant) and BYL (Tent, 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 Ann Arbor Plastics, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ann Arbor Plastics, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Ann Arbor Plastics, Inc.

Which product codes does it file in?

What has FDA decided for it lately?