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

Device, Acupressure

Unknown
FDA source (opens on fda.gov)

MVV is the FDA product code for Device, Acupressure. As of , FDA records hold 13 510(k) clearances under this code, the most recent dated , and one recall.

Classification record

Product code
MVV
Device name
Device, Acupressure
Device class
Unclassified
Review panel
Unknown
Submission type
FDA code 7
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
13
Ingested recalls
1

Clearances, product code MVV

By decision year
13 clearances under product code MVV with a decision year between 1990 and 2022, 2004 the highest year at 3.
Show the numbers
510(k) clearances under FDA product code MVV by decision year
YearClearances
19901
20043
20051
20061
20071
20111
20121
20141
20201
20211
20221

Applicants with the most clearances

Product code MVV
Applicants holding the most 510(k) clearances under product code MVV
ApplicantClearances
Acuband, Inc.1
Apothecary Products, LLC1
Biobands Distributors, Inc.1
Doodlebug Products, LLC1
Euro-Am Pharma, Inc.1
FridaBaby LLC1
Health Ent., Inc.1
Mumease1
Pressure Point, Inc.1
Psi Health Solutions, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code