LQX — Device, Finger-Sucking Class I

FDA Device Classification

FDA product code LQX covers "Device, Finger-Sucking", a Class I medical device regulated under 21 CFR 890.3475. Submissions are reviewed by the Physical Medicine panel. At least 2 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
LQX
Device Class
Class I
Regulation Number
890.3475
Submission Type
Review Panel
DE
Medical Specialty
Physical Medicine
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K945537med et al developmentT-GUARDMarch 23, 1995
K864870levolon companyTHUMBSHELPER POWER RINGFebruary 12, 1987