510(k) K070880
K070880 is an FDA 510(k) premarket notification submitted by Etymotic Research, Inc. for the device "ER35 ERO-SCAN PRO HEARING TEST SYSTEM". The FDA issued a decision of Substantially Equivalent on June 7, 2007. The device falls under product code EWO (Audiometer), a Class II device regulated under 21 CFR 874.1050. Etymotic Research, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 7, 2007
- Date Received
- March 30, 2007
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Audiometer
- Device Class
- Class II
- Regulation Number
- 874.1050
- Review Panel
- EN
- Submission Type