# Diasol, Inc.

- Location (FDA's records): North Hollywood, CA
- FDA decisions: 10 (1999–2014): 10 510(k) clearances
- Product codes: KPO (4), FPA (3), FMI (2), FIE (1)
- Predicates its devices cite: 7 (1 its own); citations of its devices by later devices: 6 (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
- Renal Systems, Inc.: 2 (https://510kreport.com/company/renal-systems)
- International Medical Products, Inc.: 1 (https://510kreport.com/company/international-medical-products)
- Dana Laboratories: 1 (https://510kreport.com/company/dana-laboratories)
- Rockwell Medical Technologies, Inc.: 1 (https://510kreport.com/company/rockwell-medical-technologies)
- Advanced Renal Technologies, Inc.: 1 (https://510kreport.com/company/advanced-renal-technologies)

## Firms that cite its devices most
- Nipro Renal Solutions USA, Corp.: 2 (https://510kreport.com/company/nipro-renal-solutions-usa)
- Di-Chem, Inc.: 1 (https://510kreport.com/company/di-chem)
- Global Scientific Technologies, LLC: 1 (https://510kreport.com/company/global-scientific-technologies)
- Dimesol USA, LLC: 1 (https://510kreport.com/company/dimesol-usa)

## Its most-cited devices
- K130511: Citrisol Acid Concentrate (2014), cited by 4
- K993212: Dryasol Acid Concentrate Mix (1999), cited by 2

## Recent decisions
- K130511: Citrisol Acid Concentrate (Feb 10, 2014)
- K020231: Diasol-Additives (Oct 21, 2002)
- K020230: Diasol-Bicarb (Apr 23, 2002)
- K011004: Needlelok Hypodermic Needle Protection (May 24, 2001)
- K010958: Fistulok Fistula Needle Protection (May 18, 2001)
- K011003: Safesting and Safesting Hub (Apr 20, 2001)
- K993187: Shelly Protected AV Fistula Needle (Nov 5, 1999)
- K992999: Daisy Protected Scalp Vein Set (Nov 5, 1999)

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