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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Media, Reproductive
510(k) Number K003163
Device Name SYNVITRO FLUSH
Applicant
Medicult A/S
P.O. Box 262069
San Diego,  CA  92196 -2069
Applicant Contact RONALD G LEONARDI
Correspondent
Medicult A/S
P.O. Box 262069
San Diego,  CA  92196 -2069
Correspondent Contact RONALD G LEONARDI
Regulation Number884.6180
Classification Product Code
MQL  
Date Received10/10/2000
Decision Date 03/22/2001
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Obstetrics/Gynecology
510k Review Panel Obstetrics/Gynecology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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