510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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PRLClass III

Iliac Covered Stent, Arterial

Unknown
FDA source (opens on fda.gov)

PRL is the FDA product code for Iliac Covered Stent, Arterial, a class III device type. FDA's definition for this code reads: "For the treatment of de novo or restenotic lesions found in iliac arteries". As of , FDA records hold no 510(k) clearances under this code and 6 recalls.

Classification record

Product code
PRL
Device name
Iliac Covered Stent, Arterial
FDA definition
For the treatment of de novo or restenotic lesions found in iliac arteries
Device class
Class III
Review panel
Unknown
Submission type
PMA
Implant
Yes
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
0
Ingested recalls
6

Companies listing this code with FDA

Companies whose registered establishments list this code