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

Vibrator For Therapeutic Use, Genital

21 CFR 884.5960 / Obstetrics/Gynecology
FDA source (opens on fda.gov)

KXQ is the FDA product code for Vibrator For Therapeutic Use, Genital, a class II device type, regulated under 21 CFR 884.5960. As of , FDA records hold 4 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
KXQ
Device name
Vibrator For Therapeutic Use, Genital
Regulation
21 CFR 884.5960
Device class
Class II
Review panel
Obstetrics/Gynecology
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
4
Ingested recalls
0

Clearances, product code KXQ

By decision year
4 clearances under product code KXQ with a decision year between 1996 and 2014, 1996 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code KXQ by decision year
YearClearances
19961
20011
20111
20141

Applicants with the most clearances

Product code KXQ
Applicants holding the most 510(k) clearances under product code KXQ
ApplicantClearances
Multicept, ApS.2
Reflexonic, LLC2

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 34 companies shown, in name order