FDA applicant

Respiratory Marketing, Inc.

Walker, MI1 decision1981–19810 recalls

FDA records 1 decision for Respiratory Marketing, Inc. (Walker, MI) in 1981: 1 510(k) clearance. All are in product code CAW (Generator, Oxygen, Portable). 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 Respiratory Marketing, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Respiratory Marketing, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Respiratory Marketing, 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 “Respiratory”

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

Respiratory Support Products, Inc. 27 Respiratory Care, Inc. 26 Respiratory Motion, Inc. 5 Respiratory Delivery Systems, Inc. 2 Respiratory Technologies, Incorporated 1 Respiratory Therapy 1

Respiratory Marketing, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Respiratory”