TINNITUS THERAPY SYSTEM ANM T30 CR— 510(k) K112752

Name: FDA 510(k) clearance K112752
Creator: U.S. Food and Drug Administration
Published: 2011-12-16

Substantially Equivalent

Anm Adaptive Neuromodulation GmbH

FDA 510(k) clearance K112752 for TINNITUS THERAPY SYSTEM ANM T30 CR, Substantially Equivalent on 2011-12-16. Applicant: Anm Adaptive Neuromodulation GmbH. Device class: 2.

Clearance details

Applicant: Anm Adaptive Neuromodulation GmbH
Product code: Code KLW
Device class: Class 2
Regulation: 21 CFR 874.3400
Advisory panel: Ear, Nose, Throat
Date received: 2011-09-21
Decision date: 2011-12-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Koln, DE

Download summary PDF View on FDA.gov ↗

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