EAQ — Detector, Ultraviolet Class II

FDA Device Classification

FDA product code EAQ covers "Detector, Ultraviolet", a Class II medical device regulated under 21 CFR 872.6350. Submissions are reviewed by the Dental panel. At least 2 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
EAQ
Device Class
Class II
Regulation Number
872.6350
Submission Type
Review Panel
DE
Medical Specialty
Dental
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K934728sunsorSUNSOR ULTRAVIOLET METERJuly 28, 1994
K770685parker laboratoriesLIGHT, EXAMINING, DENTAL, ULTRA VIOLETApril 26, 1977