510(k) Report

FDA applicant

Cygnus Research Corp.

Mchenry, IL5 decisions1983–19830 recalls

FDA records 5 decisions for Cygnus Research Corp. (Mchenry, IL) in 1983: 5 510(k) clearances. Most are in product codes BZO (Set, Tubing And Support, Ventilator (W Harness)) and BTT (Humidifier, Respiratory Gas, (Direct Patient…). 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 Cygnus Research Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Cygnus Research Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Cygnus”

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