510(k) Report

FDA applicant

Comfort Strap Co.

Egan, SD1 decision1988–19880 recalls

FDA records 1 decision for Comfort Strap Co. (Egan, SD) in 1988: 1 510(k) clearance. All are in product code CAT (Cannula, Nasal, Oxygen). 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 Comfort Strap Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Comfort Strap Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Comfort”

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