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

Occluder, Patent Ductus, Arteriosus

Unknown
FDA source (opens on fda.gov)

MAE is the FDA product code for Occluder, Patent Ductus, Arteriosus, a class III device type. As of , FDA records hold no 510(k) clearances under this code and 5 recalls.

Classification record

Product code
MAE
Device name
Occluder, Patent Ductus, Arteriosus
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
5

Companies listing this code with FDA

Companies whose registered establishments list this code