PEQ — Accessories To Examination Light Class I

FDA Device Classification

FDA product code PEQ covers "Accessories To Examination Light", a Class I medical device regulated under 21 CFR 880.6320. Submissions are reviewed by the General Hospital panel. At least 1 recent 510(k) clearance has been granted under this product code.

Classification Details

Product Code
PEQ
Device Class
Class I
Regulation Number
880.6320
Submission Type
Review Panel
HO
Medical Specialty
General Hospital
Implant
No

Definition

Accessories that attach to the light and assist in magnifying, clarifying, enhancing the image being viewed.

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K131338globalmedia groupDERMA HOODJuly 10, 2013