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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Dilator, Vessel, For Percutaneous Catheterization
510(k) Number K840022
Device Name HEART CATHETERIZATION TRAY SET
Applicant
Medi-Plast Intl., Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Medi-Plast Intl., Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number870.1310
Classification Product Code
DRE  
Date Received01/05/1984
Decision Date 02/04/1984
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Cardiovascular
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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