510(k) Report

FDA applicant

Cybermedic, Inc.

Mchenry, IL11 decisions1979–19940 recalls

FDA records 11 decisions for Cybermedic, Inc. (Mchenry, IL) from 1979 to 1994: 11 510(k) clearances. Most are in product codes BZC (Calculator, Pulmonary Function Data) and BZM (Calculator, Pulmonary Function Interpretor…). 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 Cybermedic, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Cybermedic, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Cybermedic, Inc.’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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