# Bionetic Laboratory Products

- Location (FDA's records): Mchenry, IL
- FDA decisions: 8 (1983–1984): 8 510(k) clearances
- Product codes: JTQ (2), LHL (2), LJK (1), KHW (1), LFY (1), GLZ (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K833637: VZV Bio-Enzabead Screen Kit (Feb 10, 1984)
- K832900: Immunoenzyme Test Sys-Detect-Igm Anti (Nov 14, 1983)
- K832069: Toxo Ipa Kit Ian Indirect Fluorescent (Sep 26, 1983)
- K831760: Legionella Ifa Kit I (Aug 8, 1983)
- K831133: Amebiasis Bio-Enzabead Screen Kit (Jun 8, 1983)
- K830820: Legionella Dfa Kit I (Jun 8, 1983)
- K830405: Lbi-100 37DEGREES Incubator (Mar 10, 1983)
- K830227: Automated Elisa Reader Lbi 300 (Mar 10, 1983)

Source page: https://510kreport.com/company/bionetic-laboratory-products