Viberect Penile Vibratory Stimulation Device— 510(k) K142304

Substantially Equivalent

Reflexonic, LLC

FDA 510(k) clearance K142304 for Viberect Penile Vibratory Stimulation Device, Substantially Equivalent on 2014-10-03. Applicant: Reflexonic, LLC.

Clearance details

Applicant: Reflexonic, LLC
Product code: Code KXQ
Advisory panel: Obstetrics/Gynecology
Date received: 2014-08-18
Decision date: 2014-10-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Frederick, MD, US

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