FDA product code PZV: Peripheral Blood Processing Device For Clinical Use
PZV is the FDA product code for peripheral blood processing device for clinical use. It is a Not classified device, reviewed by the Hematology panel. Devices under PZV reach the market by Contact FDA; FDA lists no cleared 510(k)s for it.
Definition
Preparation of autologous platelet rich plasma from a small sample of peripheral blood for clinical use
Classification
| Field | Value |
|---|---|
| Device name | Peripheral Blood Processing Device For Clinical Use |
| Device class | Not classified |
| Review panel | HE — Hematology |
| Medical specialty | Unknown |
| Premarket route | Contact FDA |
Recalls for PZV devices
openFDA lists no recalls for product code PZV.
Frequently asked questions
What is FDA product code PZV?
PZV is the FDA product code for peripheral blood processing device for clinical use. It is a Not classified device, reviewed by the Hematology panel.
What device class is PZV?
Not classified. Typical premarket route: Contact FDA.
Next steps
- Run an FDA pathway report with predicate devices for product code PZV
- Run a recall and safety report across every PZV manufacturer
- Watch product code PZV for new clearances and recalls
Source: openFDA device classification, 510(k), PMA, De Novo and recall data (public domain). Review days run from FDA receipt to decision. Not regulatory advice.