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

Device, Inflation, Middle Ear

Unknown
FDA source (opens on fda.gov)

MJV is the FDA product code for Device, Inflation, Middle Ear. As of , FDA records hold 6 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
MJV
Device name
Device, Inflation, Middle Ear
Device class
Unclassified
Review panel
Unknown
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
6
Ingested recalls
0

Clearances, product code MJV

By decision year
6 clearances under product code MJV with a decision year between 1992 and 2026, 1992 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code MJV by decision year
YearClearances
19921
19951
20081
20211
20231
20261

Applicants with the most clearances

Product code MJV
Applicants holding the most 510(k) clearances under product code MJV
ApplicantClearances
Abigo Medical AB1
Arisil Medical1
Earflo Company1
Exercore, LLC1
Micromedics, Inc.1
Ningbo Albert Novosino Co., Ltd.1

Companies listing this code with FDA

Companies whose registered establishments list this code