FDA device listing
Anesthetic Gel Adapter,Dual Check Valve,Dual Male Luer Lock Adapter,Endoscopic Tuohy Borst Adapter,Female Luer Lock…
FDA device listing 1479339058 · COOK, INC.
Key facts
| Proprietary names | Anesthetic Gel Adapter,Dual Check Valve,Dual Male Luer Lock Adapter,Endoscopic Tuohy Borst Adapter,Female Luer Lock Cap,Universal Check Flo Adapter |
|---|---|
| Owner/operator | COOK, INC. |
| Owner/operator number | 1820334 |
| Product codes | EYK |
| Device names | EYK - Connector, Ureteral Catheter |
| Device class | Class I |
| Classification regulations (21 CFR) | 876.5130 |
| Review panels | Gastroenterology & Urology |
| Registered establishments | Cook Incorporated |
| Establishment registrations | 1820334, 1825146 |
| FEI numbers | 1820334, 1825146 |
| Establishment operations | Complaint File Establishment, 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