510(k) K090579
K090579 is an FDA 510(k) premarket notification submitted by Intelligent Hearing Systems for the device "SMARTSCREENER-PLUS2". The FDA issued a decision of Substantially Equivalent on July 7, 2009. The device falls under product code GWJ (Stimulator, Auditory, Evoked Response), a Class II device regulated under 21 CFR 882.1900. Intelligent Hearing Systems has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 7, 2009
- Date Received
- March 3, 2009
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Stimulator, Auditory, Evoked Response
- Device Class
- Class II
- Regulation Number
- 882.1900
- Review Panel
- NE
- Submission Type