FDA applicant

Responsive Respiratory

St. Louis, MO2 decisions2006–20250 recalls

FDA records 2 decisions for Responsive Respiratory (St. Louis, MO) from 2006 to 2025: 2 510(k) clearances. Most are in product codes NFB (Conserver, Oxygen) and CAN (Regulator, Pressure, Gas Cylinder). Its devices cite 6 predicates, 0 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “Responsive Respiratory, Inc.”.

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 Responsive Respiratory’s devices, and how often a recall has named them.

FDA decisions per year

1in 2025

2007high 1 (2025) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Responsive Respiratory’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Responsive”

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

Responsive Arthroscopy, LLC 13 Responsive Orthopedics, LLC 2

Responsive Respiratory

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Responsive”