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

Device, Detection, Sulfide

21 CFR 872.1870 / Dental
FDA source (opens on fda.gov)

MVH is the FDA product code for Device, Detection, Sulfide, a class II device type, regulated under 21 CFR 872.1870. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and one recall.

Classification record

Product code
MVH
Device name
Device, Detection, Sulfide
Regulation
21 CFR 872.1870
Device class
Class II
Review panel
Dental
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
1
Ingested recalls
1

Clearances, product code MVH

By decision year
1 clearance under product code MVH with a decision year between 1998 and 1998, 1998 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code MVH by decision year
YearClearances
19981

Applicants with the most clearances

Product code MVH
Applicants holding the most 510(k) clearances under product code MVH
ApplicantClearances
Diamond General Development Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code

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