FDA applicant

Inhalation Plastics

Chicago, IL7 decisions1988–19950 recalls

FDA records 7 decisions for Inhalation Plastics (Chicago, IL) from 1988 to 1995: 7 510(k) clearances. Most are in product codes CAI (Circuit, Breathing (W Connector, Adaptor, Y…) and BTT (Humidifier, Respiratory Gas, (Direct Patient…). 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 Inhalation Plastics’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Inhalation Plastics since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

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Other applicant names beginning “Inhalation”

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

Inhalation Therapy Equipment, Co. 3

Inhalation Plastics

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Inhalation”