# Bio-Rad Laboratories, Inc., Clinical Systems Divis

- Location (FDA's records): Hercules, CA
- FDA decisions: 3 (2012–2013): 3 510(k) clearances
- Product codes: LCP (3)
- Predicates its devices cite: 4 (1 its own); citations of its devices by later devices: 1 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Bio-Rad Laboratories, Inc.: 2 (https://510kreport.com/company/bio-rad-laboratories)
- Bio-Rad Laboratories Inc., Clinical Systems Divisi: 1 (https://510kreport.com/company/bio-rad-laboratories-clinical-systems-divisi)

## Its most-cited devices
- K122472: Variant II Turbo HBA1C Kit-2.0 Variant II Turbo Hemoglobin Testing System (2012), cited by 1

## Recent decisions
- K130990: Variant (TM) II Turbo HBA1C Kit - 2.0 (May 9, 2013)
- K130860: Variant II Hemoglobin A1C Program (New), Variant II Hemoglobin Testing System with CDM Software, CDM Software (Apr 25, 2013)
- K122472: Variant II Turbo HBA1C Kit-2.0 Variant II Turbo Hemoglobin Testing System (Oct 26, 2012)

Source page: https://510kreport.com/company/bio-rad-laboratories-clinical-systems-divis