510(k) K963838
K963838 is an FDA 510(k) premarket notification submitted by Starkey Laboratories, Inc. for the device "STARKEY TM AIR CONDUCTION TINNITUS MASKER". The FDA issued a decision of Substantially Equivalent on November 26, 1996. The device falls under product code KLW (Masker, Tinnitus), a Class II device regulated under 21 CFR 874.3400. Starkey Laboratories, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- November 26, 1996
- Date Received
- September 24, 1996
- 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