DeviceClearance

ELITONE Urge Urinary Incontinence Device— 510(k) K223884

Substantially Equivalent

Elidah, Inc.

FDA 510(k) clearance K223884 for ELITONE Urge Urinary Incontinence Device, Substantially Equivalent on 2023-02-24. Applicant: Elidah, Inc..

Clearance details

Applicant
Elidah, Inc.
Product code
Code QAJ
Advisory panel
Gastroenterology, Urology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Monroe, CT, US
Download summary PDFView on FDA.gov ↗

Data sourced from openFDA. This site is unofficial and independent of the FDA.