FDA device listing
Leica FL800 ULT
FDA device listing 1052119132 · Leica Microsystems CMS GmbH
Key facts
| Proprietary names | Leica FL800 ULT |
|---|---|
| Owner/operator | Leica Microsystems CMS GmbH |
| Owner/operator number | 10054809 |
| Premarket submissions | K141136 |
| Product codes | IZI |
| Device names | IZI - System, X-Ray, Angiographic |
| Device class | Class II |
| Classification regulations (21 CFR) | 892.1600 |
| Review panels | Radiology |
| Registered establishments | LEICA INSTRUMENTS (SINGAPORE) PTE LTD., LEICA MICROSYSTEMS (SCHWEIZ) AG |
| Establishment registrations | 1000204638, 3003974370 |
| FEI numbers | 1000204638, 3003974370 |
| Establishment operations | Contract Manufacturer, Specification Developer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- None 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