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