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

Kit, Typing, Hla-Dqb

21 CFR 866.5660 / Immunology
FDA source (opens on fda.gov)

MVS is the FDA product code for Kit, Typing, Hla-Dqb, a class II device type, regulated under 21 CFR 866.5660. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
MVS
Device name
Kit, Typing, Hla-Dqb
Regulation
21 CFR 866.5660
Device class
Class II
Review panel
Immunology
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
1
Ingested recalls
0

Clearances, product code MVS

By decision year
1 clearance under product code MVS with a decision year between 2002 and 2002, 2002 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code MVS by decision year
YearClearances
20021

Applicants with the most clearances

Product code MVS
Applicants holding the most 510(k) clearances under product code MVS
ApplicantClearances
Cheshire Diagnostics, Ltd.1

Companies listing this code with FDA

Companies whose registered establishments list this code

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