FDA applicant

Gibeck Respiration

Schaumburg, IL6 decisions1987–19880 recalls

FDA records 6 decisions for Gibeck Respiration (Schaumburg, IL) from 1987 to 1988: 6 510(k) clearances. All are in product code BYD (Condenser, Heat And Moisture (Artificial Nose)). 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 Gibeck Respiration’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Gibeck Respiration since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Gibeck”

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

Gibeck, Inc. 15

Gibeck Respiration

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Gibeck”