FDA device listing
Eau de Quinton - Quinton Action Plus Nasal Hygiene 100ml, 150ml,Eau de Quinton - Quinton Daily Nasal Hygiene 100ml…
FDA device listing 1157859217 · Laboratories Quinton International S. L.
Key facts
| Proprietary names | Eau de Quinton - Quinton Action Plus Nasal Hygiene 100ml, 150ml,Eau de Quinton - Quinton Daily Nasal Hygiene 100ml, 150ml,Eau de Quinton - Quinton Pediatric Nasal Hygiene 100ml |
|---|---|
| Owner/operator | Laboratories Quinton International S. L. |
| Owner/operator number | 10086890 |
| Product codes | KCO |
| Device names | KCO - Nasal Spray, Ent Delivery |
| Device class | Class I |
| Classification regulations (21 CFR) | 874.5220 |
| Review panels | Ear, Nose, & Throat |
| Registered establishments | LABORATORIES QUINTON INTERNATIONAL S. L. |
| Establishment registrations | 3025604927 |
| FEI numbers | 3025604927 |
| 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