FDA device listing
Interlink Blunt Plastic Cannula
FDA device listing 2035939117 · Becton Dickinson and Company
Key facts
| Proprietary names | Interlink Blunt Plastic Cannula |
|---|---|
| Owner/operator | Becton Dickinson and Company |
| Owner/operator number | 9922032 |
| Premarket submissions | K974363 |
| Product codes | FMI |
| Device names | FMI - Needle, Hypodermic, Single Lumen |
| Device class | Class II |
| Classification regulations (21 CFR) | 880.5570 |
| Review panels | General Hospital |
| Registered establishments | Becton, DIckinson and Company, BECTON DICKINSON AND COMPANY, BECTON DICKINSON INFUSION THERAPY SYSTEMS INC. |
| Establishment registrations | 1213809, 1710034, 1911916 |
| FEI numbers | 1213809, 1710034, 1911916 |
| Establishment operations | Manufacturer, Specification Developer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 1–9 UDI devices (GUDID) under the same submission
- 1–9 Device listings citing the same submission
- Yes 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