FDA applicant

Mckesson Corp.

Mchenry, IL5 decisions1976–19770 recalls

FDA records 5 decisions for Mckesson Corp. (Mchenry, IL) from 1976 to 1977: 5 510(k) clearances. Most are in product codes CAO (Airway, Esophageal (Obturator)) and BZR (Mixer, Breathing Gases, Anesthesia Inhalation). 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 Mckesson Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Mckesson Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Mckesson”

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

Mckesson Israel, Ltd. 5 Mckesson Medical Imaging Company 3 Mckesson Information Solutions, LLC 1 Mckesson Technologies, Inc. 1

Mckesson Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Mckesson”