510(k) K982249

INTERACOUSTICS MODEL AD229 DIAGNOSTIC AUDIOMETER by Idem (Int'L Dist. of Electronics For Medicine) — Product Code EWO

K982249 is an FDA 510(k) premarket notification submitted by Idem (Int'L Dist. of Electronics For Medicine) for the device "INTERACOUSTICS MODEL AD229 DIAGNOSTIC AUDIOMETER". The FDA issued a decision of Substantially Equivalent on August 7, 1998. The device falls under product code EWO (Audiometer), a Class II device regulated under 21 CFR 874.1050. Idem (Int'L Dist. of Electronics For Medicine) has at least 5 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 7, 1998
Date Received
June 26, 1998
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