FDA product code PQV: ß-Glucocerebrosidase (Gba) Newborn Screening Test System
PQV is the FDA product code for ß-glucocerebrosidase (gba) newborn screening test system. It is a Class II device, regulated under 21 CFR 862.1488 and reviewed by the Clinical Chemistry panel. Devices under PQV reach the market by 510(k); FDA lists no cleared 510(k)s for it.
Definition
For quantitative measurement of the activity of ß-glucocerebrosidase (GBA) from newborn dried blood spot specimens.
Classification
| Field | Value |
|---|---|
| Device name | ß-Glucocerebrosidase (Gba) Newborn Screening Test System |
| Device class | Class II |
| Regulation | 21 CFR 862.1488 |
| Review panel | CH — Clinical Chemistry |
| Medical specialty | Clinical Chemistry |
| Premarket route | 510(k) |
| Third-party 510(k) review eligible | Yes |
Recalls for PQV devices
openFDA lists no recalls for product code PQV.
Frequently asked questions
What is FDA product code PQV?
PQV is the FDA product code for ß-glucocerebrosidase (gba) newborn screening test system. It is a Class II device, regulated under 21 CFR 862.1488 and reviewed by the Clinical Chemistry panel.
What device class is PQV?
Class II, regulation 21 CFR 862.1488. Typical premarket route: 510(k).
Next steps
- Run an FDA pathway report with predicate devices for product code PQV
- Run a recall and safety report across every PQV manufacturer
- Watch product code PQV 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.
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