FDA applicant
Microbiological Assoc.
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
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.
Planning a device like Microbiological Assoc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) ReportOther applicant names beginning “Microbiological”
FDA records each applicant name separately; these may or may not be the same firm.