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

Device, Hemostasis, Vascular

Unknown
FDA source (opens on fda.gov)

MGB is the FDA product code for Device, Hemostasis, Vascular, a class III device type. As of , FDA records hold no 510(k) clearances under this code and 12 recalls.

Classification record

Product code
MGB
Device name
Device, Hemostasis, Vascular
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
12

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 23 companies shown, in name order