FDA device listing
Reprocessed EP Catheter and Cable
FDA device listing 1189057655 · STRYKER CORP.
Key facts
| Proprietary names | Reprocessed EP Catheter and Cable |
|---|---|
| Owner/operator | STRYKER CORP. |
| Owner/operator number | 1811755 |
| Premarket submissions | K030187 |
| Product codes | DSA, NLH |
| Device names | DSA - Cable, Transducer And Electrode, Patient, (Including Connector), NLH - Catheter, Recording, Electrode, Reprocessed |
| Device class | Class II |
| Classification regulations (21 CFR) | 870.1220, 870.2900 |
| Review panels | Cardiovascular |
| Registered establishments | Stryker Sustainability Solutions, Stryker Sustainability Solutions Phoenix |
| Establishment registrations | 2090040, 3009350690 |
| FEI numbers | 3002615969, 3009350690 |
| Establishment operations | Reprocessor of Single Use Devices, Specification Developer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 10–99 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