FDA device listing
Artisan Jones' Basement Membrane H&E (PAS-M) Stain Kit,Artisan Jones' Basement Membrane H&E Stain Kit,Artisan Jones'…
FDA device listing 1806806026 · Agilent Technologies, Inc
Key facts
| Proprietary names | Artisan Jones' Basement Membrane H&E (PAS-M) Stain Kit,Artisan Jones' Basement Membrane H&E Stain Kit,Artisan Jones' Basement Membrane Light Green (PAS-M) Stain Kit,Artisan Jones' Basement Membrane (PAS-M) Stain Kit,Artisan Jones' Basement Membrane Stain Kit,Artisan PAS-Green Stain Kit,Artisan Periodic Acid Schiff (PAS) Stain Kit |
|---|---|
| Owner/operator | Agilent Technologies, Inc |
| Owner/operator number | 10038794 |
| Product codes | HZT |
| Device names | HZT - Reagent, Schiff |
| Device class | Class I |
| Classification regulations (21 CFR) | 864.1850 |
| Review panels | Hematology |
| Registered establishments | Agilent Technologies Inc., Agilent Technologies, Inc, Agilent Technologies, Inc. |
| Establishment registrations | 2022180, 2916205, 3009189893 |
| FEI numbers | 2022180, 2916205, 3009189893 |
| Establishment operations | Complaint File Establishment, Manufacturer, Specification Developer |
| 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