FDA device listing
Pall Acrodose PLus System Platelet Pool,Store Set with in-line Leukocyte Reduction Filter
FDA device listing 1063033748 · GVS TM, Inc.
Key facts
| Proprietary names | Pall Acrodose PLus System Platelet Pool,Store Set with in-line Leukocyte Reduction Filter |
|---|---|
| Owner/operator | GVS TM, Inc. |
| Owner/operator number | 10093016 |
| Premarket submissions | BK070057 |
| Product codes | KSR |
| Device names | KSR - Container, Empty, For Collection & Processing Of Blood & Blood Components |
| Device class | Class II |
| Classification regulations (21 CFR) | 864.9100 |
| Review panels | Hematology |
| Registered establishments | GVS TM, INC. |
| Establishment registrations | 3037389071 |
| FEI numbers | 2013342 |
| Establishment operations | Manufacturer |
| 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