Sound Options Tinnitus Treatment

GUDID 00627843723226

Sound Options Tinnitus Treatments Inc

Tinnitus masking application software Tinnitus masking application software
Primary Device ID00627843723226
NIH Device Record Key124c31b8-5481-4688-ad5a-4535757e46f4
Commercial Distribution StatusIn Commercial Distribution
Brand NameSound Options Tinnitus Treatment
Version Model Number2.0
Company DUNS203087069
Company NameSound Options Tinnitus Treatments Inc
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone1-866-688-3772
Emailinfo@soundoptions.ca
Phone1-866-688-3772
Emailinfo@soundoptions.ca

Device Identifiers

Device Issuing AgencyDevice ID
GS100627843723226 [Primary]

FDA Product Code

KLWMasker, Tinnitus

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2017-02-23

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.