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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
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