510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
QANClass III

Stent, Iliac Vein

Unknown
FDA source (opens on fda.gov)

QAN is the FDA product code for Stent, Iliac Vein, a class III device type. FDA's definition for this code reads: "A metal scaffold placed via a delivery catheter in the iliac vein to maintain the lumen". As of , FDA records hold no 510(k) clearances under this code and 9 recalls.

Classification record

Product code
QAN
Device name
Stent, Iliac Vein
FDA definition
A metal scaffold placed via a delivery catheter in the iliac vein to maintain the lumen
Device class
Class III
Review panel
Unknown
Submission type
PMA
Implant
Yes
Life sustaining or supporting
Yes
GMP exempt
No
Third party review eligible
No
Ingested clearances
0
Ingested recalls
9

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 15 companies shown, in name order