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

Catheter, Coronary, Atherectomy

Unknown
FDA source (opens on fda.gov)

MCX is the FDA product code for Catheter, Coronary, Atherectomy, a class III device type. As of , FDA records hold no 510(k) clearances under this code and 14 recalls.

Classification record

Product code
MCX
Device name
Catheter, Coronary, Atherectomy
Device class
Class III
Review panel
Unknown
Submission type
PMA
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
0
Ingested recalls
14

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 15 companies shown, in name order