FDA applicant

Mckesson Technologies, Inc.

Philedelphia, PA1 decision2012–20121 recall

FDA records 1 decision for Mckesson Technologies, Inc. (Philedelphia, PA) in 2012: 1 510(k) clearance. All are in product code BSZ (Gas-Machine, Anesthesia). 1 recall is linked to its devices, 1 Class I.

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 Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2012

2012high 1 (2012) · low 0 (2013)2026

2026 so far, outlined.

Recalls per year

1in 2013

2012high 1 (2013) · low 0 (2012)2026

Class I Class II/III not classified

FIG. 1 — Mckesson Technologies, Inc. by year, 2012–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Mckesson Technologies, Inc.’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

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 Corp. 5 Mckesson Medical Imaging Company 3 Mckesson Information Solutions, LLC 1

Mckesson Technologies, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

What has been recalled?

Other applicant names beginning “Mckesson”