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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name catheter, intravascular, therapeutic, short-term less than 30 days
510(k) Number K821372
Device Name DESERET INTRACATH INTRAVENOUS CATHETER
Applicant
WARNER-LAMBERT CO.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
WARNER-LAMBERT CO.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number880.5200
Classification Product Code
FOZ  
Date Received05/10/1982
Decision Date 06/02/1982
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
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