FDA Device Intelligence
Home › Device types › PBN

Apheresis For Focal Glomerulosclerosis In Adult And Pediatric Patients

FDA product code PBN · Class f · Unknown

5
Registered devices
29
Adverse events
0
Recalls
0
510(k) clearances

Devices with this code

TUBING SYSTEM FOR PLASMAPHERESIS — KANEKA PHARMA AMERICA LLCTUBING SYSTEM FOR PLASMAPHERESIS — KANEKA PHARMA AMERICA LLCLIPOSORBER — KANEKA CORPORATIONAPHERESIS MACHINE — KANEKA PHARMA AMERICA LLCSULFLUX — KANEKA PHARMA AMERICA LLC

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.