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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Implant, Endosseous, Root-Form
510(k) Number K873255
Device Name THE MICRO-VENT/HA
Applicant
Core-Vent Corp.
15821 Ventura Blvd.
Encino,  CA  91436
Applicant Contact GERALD NIZNICK
Correspondent
Core-Vent Corp.
15821 Ventura Blvd.
Encino,  CA  91436
Correspondent Contact GERALD NIZNICK
Regulation Number872.3640
Classification Product Code
DZE  
Date Received08/17/1987
Decision Date 03/14/1988
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Dental
510k Review Panel Dental
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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