FDA device listing
Atellica IM Folate Assay (FOL),Atellica IM Folate Diluent (FOL DIL),Atellica IM Folate DTT/Releasing Agent (Fol…
FDA device listing 1180601157 · SIEMENS HEALTHCARE DIAGNOSTICS INC.
Key facts
| Proprietary names | Atellica IM Folate Assay (FOL),Atellica IM Folate Diluent (FOL DIL),Atellica IM Folate DTT/Releasing Agent (Fol DTT/REL),Atellica IM Folate RBC (Fol RBC) |
|---|---|
| Owner/operator | SIEMENS HEALTHCARE DIAGNOSTICS INC. |
| Owner/operator number | 9096044 |
| Premarket submissions | K172201 |
| Product codes | CGN |
| Device names | CGN - Acid, Folic, Radioimmunoassay |
| Device class | Class II |
| Classification regulations (21 CFR) | 862.1295 |
| Review panels | Clinical Chemistry |
| Registered establishments | Siemens Healthcare Diagnostics Inc. |
| Establishment registrations | 1219913, 2432235 |
| FEI numbers | 1219913, 2432235 |
| Establishment operations | Complaint File Establishment, Specification Developer, Manufacturer |
| 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