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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Instrument, Manual, Specialized Obstetric-Gynecologic
510(k) Number K062438
Device Name BAKRI POSTPARTUM BALLOON, MODEL J-SOS-100500
Applicant
Cook Ob/Gyn
1100 W. Morgan St.
Spencer,  IN  47460
Applicant Contact CINDY RUMPLE
Correspondent
Cook Ob/Gyn
1100 W. Morgan St.
Spencer,  IN  47460
Correspondent Contact CINDY RUMPLE
Regulation Number884.4530
Classification Product Code
KNA  
Date Received08/21/2006
Decision Date 10/27/2006
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
Predetermined Change
Control Plan Authorized		 No
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