OSG — Piezo-Electric Stimulator For Relief Of Mosquito Bite Itch Class II

FDA Device Classification

FDA product code OSG covers "Piezo-Electric Stimulator For Relief Of Mosquito Bite Itch", a Class II medical device regulated under 21 CFR 882.5894. Submissions are reviewed by the Neurology panel. At least 2 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
OSG
Device Class
Class II
Regulation Number
882.5894
Submission Type
Review Panel
NE
Medical Specialty
Neurology
Implant
No

Definition

Relief / Reduction of Mosquito Bite Itch

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
DEN130019tecnimedZANZA-CLICKNovember 7, 2014
DEN100024ecobrandsZAP-IT!November 7, 2014