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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name needle, assisted reproduction
510(k) Number K023930
Device Name COOPERSURGICAL OOCYTE RECOVERY NEEDLES
Applicant
COOPERSURGICAL, INC.
P.O. BOX 2156
HUNTINGTON,  CT  06484
Applicant Contact JOSEPH M AZARY
Correspondent
COOPERSURGICAL, INC.
P.O. BOX 2156
HUNTINGTON,  CT  06484
Correspondent Contact JOSEPH M AZARY
Regulation Number884.6100
Classification Product Code
MQE  
Date Received11/25/2002
Decision Date 01/22/2003
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Obstetrics/Gynecology
510k Review Panel Obstetrics/Gynecology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
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