510(k) K003559

TCI (TINNITUS CONTROL INSTRUMENT) by Siemens Hearing Instruments, Inc. — Product Code KLW

K003559 is an FDA 510(k) premarket notification submitted by Siemens Hearing Instruments, Inc. for the device "TCI (TINNITUS CONTROL INSTRUMENT)". The FDA issued a decision of Substantially Equivalent on April 26, 2001. The device falls under product code KLW (Masker, Tinnitus), a Class II device regulated under 21 CFR 874.3400. Siemens Hearing Instruments, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 26, 2001
Date Received
November 17, 2000
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

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