510(k) Report

FDA applicant

Microbiological Assoc.

Mchenry, IL8 decisions1977–19800 recalls

FDA records 8 decisions for Microbiological Assoc. (Mchenry, IL) from 1977 to 1980: 8 510(k) clearances. Most are in product codes GOK (Antisera, Hai (Including Hai Control), Rubella) and KIT (Media And Components, Synthetic Cell 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 Microbiological Assoc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Microbiological Assoc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Microbiological”

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