← FDA DEVICE PRODUCT CODES

FDA PRODUCT CODE · CLASS III

QAN — Stent, Iliac Vein

A metal scaffold placed via a delivery catheter in the iliac vein to maintain the lumen

DEVICE CLASS
Class III
MEDICAL SPECIALTY
Unknown
REVIEW PANEL
CV
✓ Implant✓ Life-sustaining— GMP-exempt— Third-party review eligible
4
510(K)/PMA CLEARANCES
pma: 4
0
RECALL ENTRIES

Recent clearances

P180037Bard Peripheral Vascular, Inc. · pma2026-06-10
P200026Medtronic Vascular, Inc. · pma2026-04-27
P200023Cook Ireland, Ltd. · pma2026-04-14
P230021Philips Image Guided Therapy Corporation · pma2026-02-12

Related on SPEQ

Medical devices industry →Medical device quality (ISO 13485) →FDA device clearances →FDA enforcement & recalls →

Source: FDA device classification, 510(k)/PMA, and recall datasets (openFDA). Recall entries count distinct FDA recall numbers, so one recall event affecting several products appears as several entries. SPEQ is not affiliated with the FDA; this is a reference view of public FDA data.

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