FDA applicant

Minnesota Resuscitation Solutions, D.B.D Advancedcpr Solutio

Edina, MN1 decision2020–20200 recalls

FDA records 1 decision for Minnesota Resuscitation Solutions, D.B.D Advancedcpr Solutio (Edina, MN) in 2020: 1 510(k) clearance. All are in product code FOA (Board, Cardiopulmonary). 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, general hospital panel, where it files most

How often FDA has decided Minnesota Resuscitation Solutions, D.B.D Advancedcpr Solutio’s devices, and how often a recall has named them.

FDA decisions per year

1in 2020

2020high 1 (2020) · low 0 (2021)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2020.

FIG. 1 — Minnesota Resuscitation Solutions, D.B.D Advancedcpr Solutio by year, 2020–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Minnesota”

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

Minnesota Laser Corp. 12 Minnesota Mining and Mfg. Co. 9 Minnesota Scientific, Inc. 5 Minnesota Valley Engineering, Inc. 4 Minnesota Medical Development, Inc. 3 Minnesota Prophy Power, Inc. 2 Minnesota Medical Technologies 1 The Minnesota Back Brace Co. 1

Minnesota Resuscitation Solutions, D.B.D Advancedcpr Solutio

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Minnesota”