510(k) Report

FDA applicant

Los Angeles Biological Products

Mchenry, IL4 decisions1979–19790 recalls

FDA records 4 decisions for Los Angeles Biological Products (Mchenry, IL) in 1979: 4 510(k) clearances. Most are in product codes JSE (Culture Media, Multiple Biochemical Test) and JSF (Culture Media, Single Biochemical Test). 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, microbiology panel, where it files most

How often FDA has decided Los Angeles Biological Products’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Los Angeles Biological Products since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Los Angeles Biological Products 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?

  • JSECulture Media, Multiple Biochemical Test2decisions
  • JSFCulture Media, Single Biochemical Test1decision
  • JSHCulture Media, Non-Selective And Differential1decision

What has FDA decided for it lately?

  • K790229Vaginalis, HaemophilusLos Angeles Biological Products · 1979
  • K790230Dentrification Lactose AgarLos Angeles Biological Products · 1979
  • K790231Decarboxylase, Buffered LysineLos Angeles Biological Products · 1979
  • K790232Agar, Motility-NitrateLos Angeles Biological Products · 1979

All 4 as Los Angeles Biological Products →