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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Set, Administration, Intravascular
510(k) Number K781744
Device Name IV SET WITH GRADUATED CHAMBER
Applicant
NATIONAL PATENT DEVELOPMENT CORP.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
NATIONAL PATENT DEVELOPMENT CORP.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number880.5440
Classification Product Code
FPA  
Date Received10/20/1978
Decision Date 12/07/1978
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
Recalls CDRH Recalls
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