510(k) Report

FDA applicant

C-V Monitors Corp.

Mchenry, IL5 decisions1978–19790 recalls

FDA records 5 decisions for C-V Monitors Corp. (Mchenry, IL) from 1978 to 1979: 5 510(k) clearances. Most are in product codes DSF (Recorder, Paper Chart) and DRQ (Amplifier And Signal Conditioner, Transducer…). 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, cardiovascular panel, where it files most

How often FDA has decided C-V Monitors Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for C-V Monitors Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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