FDA applicant

Respirizer Co., Div. Campillary Systems, Inc.

Mchenry, IL1 decision1981–19810 recalls

FDA records 1 decision for Respirizer Co., Div. Campillary Systems, Inc. (Mchenry, IL) in 1981: 1 510(k) clearance. All are in product code KFZ (Humidifier, Non-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 Respirizer Co., Div. Campillary Systems, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Respirizer Co., Div. Campillary Systems, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Respirizer Co., Div. Campillary Systems, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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

See the 510(k) Report

Respirizer Co., Div. Campillary Systems, Inc.

Which product codes does it file in?

What has FDA decided for it lately?