510(k) Report

FDA applicant

Acumed Technologies, Inc.

Waukesha, WI1 decision1988–19880 recalls

FDA records 1 decision for Acumed Technologies, Inc. (Waukesha, WI) in 1988: 1 510(k) clearance. All are in product code CCK (Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase). 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 Acumed Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Acumed Technologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Acumed 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 “Acumed”

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