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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Disk, Abrasive
510(k) Number K873002
Device Name MIN-IDENTOFLEX
Applicant
Centrix, Inc.
30 Stran Rd.
Milford,  CT  06460
Applicant Contact JOHN DISCKO
Correspondent
Centrix, Inc.
30 Stran Rd.
Milford,  CT  06460
Correspondent Contact JOHN DISCKO
Regulation Number872.6010
Classification Product Code
EHJ  
Date Received08/04/1987
Decision Date 08/17/1987
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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