510(k) Report

FDA applicant

Modern Medical Systems Co.

Mchenry, IL2 decisions1980–19800 recalls

FDA records 2 decisions for Modern Medical Systems Co. (Mchenry, IL) in 1980: 2 510(k) clearances. Most are in product codes BTT (Humidifier, Respiratory Gas, (Direct Patient…) and BTM (Ventilator, Emergency, Manual (Resuscitator)). 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 Modern Medical Systems Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Modern Medical Systems Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Modern Medical Systems Co.’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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Other applicant names beginning “Modern”

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