FDA applicant

Porta-Lung Co.

Mchenry, IL1 decision1984–19840 recalls

FDA records 1 decision for Porta-Lung Co. (Mchenry, IL) in 1984: 1 510(k) clearance. All are in product code BYT (Ventilator, External Body, Negative Pressure…). 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 Porta-Lung Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Porta-Lung Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Porta-Lung Co.’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 “Porta-Lung”

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

Porta Ray, Inc. 4 Porta-Pro, Inc. 1 Porta-Stat, Inc. 1

Porta-Lung Co.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Porta-Lung”