510(k) Report

FDA applicant

Minnesota Valley Engineering, Inc.

New Prague, MN4 decisions1987–19880 recalls

FDA records 4 decisions for Minnesota Valley Engineering, Inc. (New Prague, MN) from 1987 to 1988: 4 510(k) clearances. All are in product code BYJ (Unit, Liquid-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 Minnesota Valley Engineering, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Minnesota Valley Engineering, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • BYJUnit, Liquid-Oxygen, Portable4decisions

What has FDA decided for it lately?

  • K882328HI Flow 50Minnesota Valley Engineering, Inc. · 1988
  • K875352HI Flow Portable Liquid Oxygen UnitMinnesota Valley Engineering, Inc. · 1988
  • K880101Liberator 53/Stroller 50Minnesota Valley Engineering, Inc. · 1988
  • K872449Nomad (Base Unit/Portable Unit)Minnesota Valley Engineering, Inc. · 1987

All 4 as Minnesota Valley Engineering, Inc. →

Other applicant names beginning “Minnesota”

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

Minnesota Laser Corp. 12Minnesota Mining and Mfg. Co. 9Minnesota Scientific, Inc. 5Minnesota Medical Development, Inc. 3Minnesota Prophy Power, Inc. 2Minnesota Resuscitation Solutions, D.B.D Advancedcpr… 1Minnesota Medical Technologies 1The Minnesota Back Brace Co. 1