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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Holder, Infant Position
510(k) Number K932636
Device Name THE TUCKER SLING
Applicant
Tucker Designs, Ltd.
P.O. Box 641117
Kenner,  LA  70064
Applicant Contact KEITH A JARRETT,JR.
Correspondent
Tucker Designs, Ltd.
P.O. Box 641117
Kenner,  LA  70064
Correspondent Contact KEITH A JARRETT,JR.
Regulation Number880.5680
Classification Product Code
FRP  
Date Received06/02/1993
Decision Date 01/26/1994
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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