FDA device listing
Low Ionic Strength Solution (LISS),Polyethylene Glycol (PEG)
FDA device listing 1820734859 · AMERICAN NATIONAL RED CROSS HEADQUARTERS
Key facts
| Proprietary names | Low Ionic Strength Solution (LISS),Polyethylene Glycol (PEG) |
|---|---|
| Owner/operator | AMERICAN NATIONAL RED CROSS HEADQUARTERS |
| Owner/operator number | 9024647 |
| Product codes | KSG |
| Device names | KSG - Media, Potentiating For In Vitro Diagnostic Use |
| Device class | Class II |
| Classification regulations (21 CFR) | 864.9600 |
| Review panels | Hematology |
| Registered establishments | AMERICAN RED CROSS DIAGNOSTIC MANUFACTURING DIVISI |
| Establishment registrations | 1177732 |
| FEI numbers | 1177732 |
| Establishment operations | Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- None listed Premarket submission listed
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device listings
Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database