FDA device listing
Reprocessed Diagnostic Electrophysiology Catheter
FDA device listing 1882888778 · Innovative Health, LLC.
Key facts
| Proprietary names | Reprocessed Diagnostic Electrophysiology Catheter |
|---|---|
| Owner/operator | Innovative Health, LLC. |
| Owner/operator number | 10048854 |
| Premarket submissions | K203655 |
| Product codes | DRF, NLH |
| Device names | DRF - Catheter, Electrode Recording, Or Probe, Electrode Recording, NLH - Catheter, Recording, Electrode, Reprocessed |
| Device class | Class II |
| Classification regulations (21 CFR) | 870.1220 |
| Review panels | Cardiovascular |
| Registered establishments | INNOVATIVE HEALTH, LLC. |
| Establishment registrations | 3011610434 |
| FEI numbers | 3011610434 |
| Establishment operations | Reprocessor of Single Use Devices |
| 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