FDA applicant

Inhalation Therapy Equipment, Co.

Mchenry, IL3 decisions1982–19823 recalls

FDA records 3 decisions for Inhalation Therapy Equipment, Co. (Mchenry, IL) in 1982: 3 510(k) clearances. Most are in product codes CAF (Nebulizer (Direct Patient Interface)) and BZO (Set, Tubing And Support, Ventilator (W Harness)). 3 recalls are linked to its devices, 3 Class I.

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 Therapy Equipment, Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Inhalation Therapy Equipment, Co. since 2007.

Recalls per year

3in 2017

2007high 3 (2017) · low 0 (2007)2026

Class I Class II/III not classified

FIG. 1 — Inhalation Therapy Equipment, 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 “Inhalation”

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

Inhalation Plastics 7

Inhalation Therapy Equipment, Co.

Which product codes does it file in?

What has FDA decided for it lately?

What has been recalled?

Other applicant names beginning “Inhalation”