FDA applicant

Sonora Respiratory Products, Inc.

Sonora, CA1 decision1987–19870 recalls

FDA records 1 decision for Sonora Respiratory Products, Inc. (Sonora, CA) in 1987: 1 510(k) clearance. All are in product code CCQ (Nebulizer, Medicinal, Non-Ventilatory (Atomizer)). 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 Sonora Respiratory Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Sonora Respiratory Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Sonora”

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

Sonora Medical Systems 2

Sonora Respiratory Products, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Sonora”