Cleared Traditional

K111293 - SOUNDCURE SERENADE TINNITUS TREATMENT SYSTEM

K111293 is an FDA 510(k) clearance for SOUNDCURE SERENADE TINNITUS TREATMENT S..., manufactured by Soundcure, Inc.. The device is a Class 2 Ear, Nose, Throat device with product code KLW cleared through the Traditional 510(k) pathway after a 110-day FDA review.

K111293 · Soundcure, Inc. · Ear, Nose, Throat device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Aug 2011
Decision
110d
Days
Class 2
Risk

K111293 is an FDA 510(k) clearance for the SOUNDCURE SERENADE TINNITUS TREATMENT SYSTEM. Classified as Masker, Tinnitus (product code KLW), Class II - Special Controls.

Submitted by Soundcure, Inc. (San Jose, US). The FDA issued a Cleared decision on August 24, 2011 after a review of 110 days - within the typical 510(k) review window.

This device falls under the Ear, Nose, Throat FDA review panel, regulated under 21 CFR 874.3400 - the FDA ear, nose and throat device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Ear, Nose, Throat review framework, consistent with the majority of Class II 510(k) submissions.

View all Soundcure, Inc. devices

FDA 510(k) Submission Details - K111293

510(k) Number K111293 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 06, 2011
Decision Date August 24, 2011
Days to Decision 110 days
Submission Type Traditional
Review Panel Ear, Nose, Throat (EN)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
20d slower than avg
Panel avg: 90d · This submission: 110d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

KLW Device Classification - Class 2, Special Controls

Product Code KLW Masker, Tinnitus
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 874.3400
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Ear, Nose, Throat devices follow this clearance model.

Regulatory Peers - KLW Masker, Tinnitus

All 60
Devices cleared under the same product code (KLW) and FDA review panel - the closest regulatory comparables to K111293.
PHONAK TINNITUS BALANCE
K123450 · Phonak, LLC · Feb 2013
MULTIFLEX TINNITUS TECHNOLOGY
K122876 · Starkey Laboratories · Oct 2012
TINNITUS THERAPY SYSTEM ANM T30 CR
K112752 · Anm Adaptive Neuromodulation GmbH · Dec 2011
IE-ZEN (IN CLEAR SERIES HEARING AID)
K110973 · Widex USA · May 2011
TINNITUS SOUND GENERATOR MODULE
K110932 · Gn Resound A/S · May 2011
EVOK 900 SERIES HEARING AID/TINNITUS MASKER OPTION DEVICE
K093715 · Magnatone Hearing Aid Corp. Dba Persona Medical · Dec 2010