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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Protector, Hearing (Insert)
510(k) Number K930203
Device Name MODEL 322 CLINICAL AUDIOMETER
Applicant
Virtual Corp.
521 SW 11th
Suite 400
Portland,  OR  97205
Applicant Contact JONATHAN D BIRCK
Correspondent
Virtual Corp.
521 SW 11th
Suite 400
Portland,  OR  97205
Correspondent Contact JONATHAN D BIRCK
Classification Product Code
EWD  
Date Received01/14/1993
Decision Date 07/08/1993
Decision Substantially Equivalent (SESE)
510k Review Panel Ear Nose & Throat
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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