510(k) Report

FDA applicant

Biomedical Research & Development Laboratories, Inc.

Oklahoma City, OK3 decisions1984–19880 recalls

FDA records 3 decisions for Biomedical Research & Development Laboratories, Inc. (Oklahoma City, OK) from 1984 to 1988: 3 510(k) clearances. Most are in product codes LCX (Kit, Test, Pregnancy, Hcg, Over The Counter) and JJR (Electrolyte Controls (Assayed And Unassayed)). 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, clinical chemistry panel, where it files most

How often FDA has decided Biomedical Research & Development Laboratories, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Biomedical Research & Development Laboratories, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Biomedical Research & Development Laboratories, 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?

  • LCXKit, Test, Pregnancy, Hcg, Over The Counter1decision
  • JJRElectrolyte Controls (Assayed And Unassayed)1decision
  • JIXCalibrator, Multi-Analyte Mixture1decision

What has FDA decided for it lately?

  • K884693Universal (TM) Ion Select Electrode StandardsBiomedical Research & Development Laboratories, Inc. · 1988
  • K881655Spectrum (TM) Blood Gas and Electrolyte ControlBiomedical Research & Development Laboratories, Inc. · 1988
  • K834474H.P.T. Home Preg. Test Kit & a.P.T.Biomedical Research & Development Laboratories, Inc. · 1984

All 3 as Biomedical Research & Development Laboratories, Inc. →