510(k) K122876

MULTIFLEX TINNITUS TECHNOLOGY by Starkey Laboratories — Product Code KLW

K122876 is an FDA 510(k) premarket notification submitted by Starkey Laboratories for the device "MULTIFLEX TINNITUS TECHNOLOGY". The FDA issued a decision of Substantially Equivalent on October 31, 2012. The device falls under product code KLW (Masker, Tinnitus), a Class II device regulated under 21 CFR 874.3400. Starkey Laboratories has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 31, 2012
Date Received
September 19, 2012
Clearance Type
Traditional
Expedited Review
No
Third Party Review
Yes

Device Classification

Device Name
Masker, Tinnitus
Device Class
Class II
Regulation Number
874.3400
Review Panel
EN
Submission Type