FDA applicant
Bionetic Laboratory Products
FDA records 8 decisions for Bionetic Laboratory Products (Mchenry, IL) from 1983 to 1984: 8 510(k) clearances. Most are in product codes JTQ (Bath, Incubators/Water, All) and LHL (Reagents, Antibody, Legionella, Direct &…). 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 Bionetic Laboratory Products’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Bionetic Laboratory Products since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Bionetic Laboratory Products’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
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