# Biorent Diagnostic, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 11 (1981–1983): 11 510(k) clearances
- Product codes: JHS (1), CFH (1), KHG (1), CFJ (1), CIX (1), CKA (1), CDO (1), KNK (1), CIT (1), CGA (1), CHH (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
- K832747: Albumin Reagent Set (Oct 14, 1983)
- K823211: CK-UV Reagent (Nov 22, 1982)
- K823060: Hemoglobin Reagent (Nov 22, 1982)
- K822494: Optimized UV-GPT Reagent Set (Sep 21, 1982)
- K822493: Optimized UV-Got Reagent Set (Sep 21, 1982)
- K822492: Optimized UV-LDH Reagent Set (Sep 17, 1982)
- K820768: Colorimetric LDH Reagent Set (Apr 14, 1982)
- K820632: Colorimetric Uric Acid Reagent Set (Mar 25, 1982)

Source page: https://510kreport.com/company/biorent-diagnostic