510(k) K011366
K011366 is an FDA 510(k) premarket notification submitted by Siemens Hearing Instruments, Inc. for the device "CUSTOM TCI-COMBI (TINNITUS CONTROL INSTRUMENT COMBINATION)". The FDA issued a decision of Substantially Equivalent on June 1, 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
- June 1, 2001
- Date Received
- May 4, 2001
- 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