# Biomedia, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 19 (1979–1982): 19 510(k) clearances
- Product codes: JSI (8), JTZ (5), JTY (3), JSH (1), JTO (1), JSG (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
- K821300: #2010 Camphylobacter Agar (Jun 2, 1982)
- K821302: #50003 Quad Diagnostic System (Jun 1, 1982)
- K821301: #50002 Quad Diagnostic System (Jun 1, 1982)
- K821108: BI Plate-XLD/Hektoen  #30012 (May 13, 1982)
- K811472: Mueller Hinton Agar, Poured Into a Plate (Jun 18, 1981)
- K811479: Chodolate Agar, Enriched (Jun 18, 1981)
- K811476: Thayer Martin Agar (Jun 18, 1981)
- K811471: Mueller Hinton Agar (Jun 18, 1981)

Source page: https://510kreport.com/company/biomedia