FDA device listing
Anterior Nares Swab,Microbrush Test Swab, NP, 100mm Breakpoint,Microbrush Test Swab, NP, 80mm Breakpoint,Nasal Swab,OP…
FDA device listing 1191120018 · Young Innovations Inc
Key facts
| Proprietary names | Anterior Nares Swab,Microbrush Test Swab, NP, 100mm Breakpoint,Microbrush Test Swab, NP, 80mm Breakpoint,Nasal Swab,OP Oropharyngeal Swab |
|---|---|
| Owner/operator | Young Innovations Inc |
| Owner/operator number | 9092605 |
| Product codes | KXG |
| Device names | KXG - Applicator, Absorbent Tipped, Sterile |
| Device class | Class I |
| Classification regulations (21 CFR) | 880.6025 |
| Review panels | General Hospital |
| Registered establishments | YOUNG MICROBRUSH LLC |
| Establishment registrations | 2134751 |
| FEI numbers | 3006308155 |
| Establishment operations | Contract Manufacturer, 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