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

Device, Finger-Sucking

21 CFR 890.3475 / Physical Medicine
FDA source (opens on fda.gov)

LQX is the FDA product code for Device, Finger-Sucking, a class I device type, regulated under 21 CFR 890.3475. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
LQX
Device name
Device, Finger-Sucking
Regulation
21 CFR 890.3475
Device class
Class I
Review panel
Physical Medicine
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
Yes
Third party review eligible
No
Ingested clearances
2
Ingested recalls
0

Clearances, product code LQX

By decision year
2 clearances under product code LQX with a decision year between 1987 and 1995, 1987 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code LQX by decision year
YearClearances
19871
19951

Applicants with the most clearances

Product code LQX
Applicants holding the most 510(k) clearances under product code LQX
ApplicantClearances
Levolon Company, Inc.1
Med et AL Development1

Companies listing this code with FDA

Companies whose registered establishments list this code