510(k) K122876
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