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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name cord, retraction
510(k) Number K092384
Device Name LIQUICORD
Applicant
CENTRIX, INC.
770 RIVER RD.
SHELTON,  CT  06484 -5458
Applicant Contact ROGER MASTRONY
Correspondent
CENTRIX, INC.
770 RIVER RD.
SHELTON,  CT  06484 -5458
Correspondent Contact ROGER MASTRONY
Classification Product Code
MVL  
Date Received08/05/2009
Decision Date 11/04/2009
Decision Substantially Equivalent (SESE)
510k Review Panel Dental
Statement Statement
Type Traditional
Reviewed by Third Party No
Combination Product No
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