The following data is part of a premarket notification filed by Etymotic Research, Inc. with the FDA for Er35 Ero-scan Pro Hearing Test System.
Device ID | K070880 |
510k Number | K070880 |
Device Name: | ER35 ERO-SCAN PRO HEARING TEST SYSTEM |
Classification | Audiometer |
Applicant | ETYMOTIC RESEARCH, INC. 2001 PENNSYLVANIA AVE. NW SUITE 950 Washington, DC 20006 |
Contact | Campbell L Tuskey |
Correspondent | Campbell L Tuskey ETYMOTIC RESEARCH, INC. 2001 PENNSYLVANIA AVE. NW SUITE 950 Washington, DC 20006 |
Product Code | EWO |
CFR Regulation Number | 874.1050 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2007-03-30 |
Decision Date | 2007-06-07 |
Summary: | summary |