FDA product code MYW: Irradiation, Blood Indicators
MYW is the FDA product code for irradiation, blood indicators. It is a Not classified device, reviewed by the Hematology panel. Devices under MYW reach the market by Contact FDA; FDA lists no cleared 510(k)s for it.
Classification
| Field | Value |
|---|---|
| Device name | Irradiation, Blood Indicators |
| Device class | Not classified |
| Review panel | HE — Hematology |
| Medical specialty | Unknown |
| Premarket route | Contact FDA |
Recalls for MYW devices
openFDA lists no recalls for product code MYW.
Frequently asked questions
What is FDA product code MYW?
MYW is the FDA product code for irradiation, blood indicators. It is a Not classified device, reviewed by the Hematology panel.
What device class is MYW?
Not classified. Typical premarket route: Contact FDA.
Next steps
- Run an FDA pathway report with predicate devices for product code MYW
- Run a recall and safety report across every MYW manufacturer
- Watch product code MYW 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.