# Waters Assoc., Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 16 (1976–1981): 16 510(k) clearances
- Product codes: KIE (4), DXG (2), FMI (1), BZL (1), DSF (1), DYG (1), KHO (1), GAA (1), DXM (1), JJQ (1), CHH (1), KRB (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
- K811975: Model 480 Variable Wavelength Ultra Viol (Jul 27, 1981)
- K802481: 7FRENCH Flow Directed Triple Lumen Cath (Oct 31, 1980)
- K801852: MRM-2 Oxygen Consumption Monitor (Aug 20, 1980)
- K801431: Pan-AM Myelogram Tray (Aug 12, 1980)
- K791661: System Controller 720 Series (Sep 24, 1979)
- K791026: 4F Sterile Balloon-Less, Catheter 913-28 (Jun 22, 1979)
- K782175: Cartridge Holder, RCM 100 (Feb 15, 1979)
- K790145: Solvent Delivery System (Feb 15, 1979)

Source page: https://510kreport.com/company/waters-assoc