FDA applicant

Energetic Pulmonary

Mchenry, IL1 decision1983–19830 recalls

FDA records 1 decision for Energetic Pulmonary (Mchenry, IL) in 1983: 1 510(k) clearance. All are in product code CAF (Nebulizer (Direct Patient Interface)). 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 Energetic Pulmonary’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Energetic Pulmonary since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Energetic Pulmonary’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 “Energetic”

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

Energetic Designs, Inc. 1

Energetic Pulmonary

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Energetic”