510(k) Report

FDA applicant

Lavco Laboratory, Inc.

Mchenry, IL3 decisions1983–19830 recalls

FDA records 3 decisions for Lavco Laboratory, Inc. (Mchenry, IL) in 1983: 3 510(k) clearances. Most are in product codes JSI (Culture Media, Selective And Differential) and JSG (Culture Media, Non-Selective And…). 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 Lavco Laboratory, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Lavco Laboratory, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Lavco Laboratory, 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?

  • JSICulture Media, Selective And Differential1decision
  • JSGCulture Media, Non-Selective And Non-Differential1decision
  • JTZCulture Media, Antimicrobial Susceptibility Test, Mueller Hinton Agar/Broth1decision

What has FDA decided for it lately?

  • K833507Prepared Tryptic Soy Agar 100 MM PlateLavco Laboratory, Inc. · 1983
  • K833506Prepared Mueller Hinton Med/100 MMLavco Laboratory, Inc. · 1983
  • K833508Prepared Macconkey AgarLavco Laboratory, Inc. · 1983

All 3 as Lavco Laboratory, Inc. →