510(k) Report

FDA applicant

Certified Respiratory Services, Inc.

Mchenry, IL2 decisions1982–19820 recalls

FDA records 2 decisions for Certified Respiratory Services, Inc. (Mchenry, IL) in 1982: 2 510(k) clearances. Most are in product codes BWF (Spirometer, Therapeutic (Incentive)) and BTI (Compressor, Air, 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 Certified Respiratory Services, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Certified Respiratory Services, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Certified Respiratory Services, Inc.’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 “Certified”

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