FDA applicant

Hogan/Cologne Ent.

Mchenry, IL1 decision1980–19800 recalls

FDA records 1 decision for Hogan/Cologne Ent. (Mchenry, IL) in 1980: 1 510(k) clearance. All are in product code BZC (Calculator, Pulmonary Function Data). 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 Hogan/Cologne Ent.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Hogan/Cologne Ent. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Hogan/Cologne Ent.’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 “Hogan/Cologne”

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

Hogan & Hartson 26 Hogan Lovells US LLP 3

Hogan/Cologne Ent.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Hogan/Cologne”