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

Balloon, Detachable, For Neurovascular Occlusion

21 CFR 882.5950 / Neurology
FDA source (opens on fda.gov)

MZQ is the FDA product code for Balloon, Detachable, For Neurovascular Occlusion, a class II device type, regulated under 21 CFR 882.5950. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
MZQ
Device name
Balloon, Detachable, For Neurovascular Occlusion
Regulation
21 CFR 882.5950
Device class
Class II
Review panel
Neurology
Submission type
510(k)
Implant
Yes
Life sustaining or supporting
Yes
GMP exempt
No
Third party review eligible
No
Ingested clearances
2
Ingested recalls
0

Clearances, product code MZQ

By decision year
2 clearances under product code MZQ with a decision year between 1998 and 1998, 1998 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code MZQ by decision year
YearClearances
19982

Applicants with the most clearances

Product code MZQ
Applicants holding the most 510(k) clearances under product code MZQ
ApplicantClearances
Target Therapeutics2

Companies listing this code with FDA

Companies whose registered establishments list this code

No registered establishment in MDM’s records lists product code MZQ.