510(k) Report

FDA applicant

Microtest

Snelleville, GA4 decisions1991–19940 recalls

FDA records 4 decisions for Microtest (Snelleville, GA) from 1991 to 1994: 4 510(k) clearances. All are in product code JSM (Culture Media, Non-Propagating Transport). 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 Microtest’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Microtest since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Microtest 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?

  • JSMCulture Media, Non-Propagating Transport4decisions

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K910526Microtest Multi Microbe MediumMicrotest · 19911cites it

What has FDA decided for it lately?

  • K941579Modified Micro Test Multi Microbe Medium (M5)Microtest · 1994
  • K921472M4-RT Transport Medium, (M4 Modification)Microtest · 1992
  • K914894Virapure, Chlamypure and MycopureMicrotest · 1991
  • K910526Microtest Multi Microbe MediumMicrotest · 1991

All 4 as Microtest →