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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name i.v. start kit
510(k) Number K871281
Device Name IV START KIT
Applicant
THE JARID GROUP, INC.
41 ASCOT DR.
WAYSIDE,  NJ  07712
Applicant Contact JOEL A MARCUS
Correspondent
THE JARID GROUP, INC.
41 ASCOT DR.
WAYSIDE,  NJ  07712
Correspondent Contact JOEL A MARCUS
Regulation Number880.5200
Classification Product Code
LRS  
Date Received03/31/1987
Decision Date 05/27/1987
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
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