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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name operating room accessories table tray
510(k) Number K890501
Device Name SECOND ASSISTANT
Applicant
3M COMPANY
CHEMOLITE BLVD. & WASHINGTON
CITY RD. 19
COTTAE GROVE,  MN  55016
Applicant Contact WILLARD D LARSON
Correspondent
3M COMPANY
CHEMOLITE BLVD. & WASHINGTON
CITY RD. 19
COTTAE GROVE,  MN  55016
Correspondent Contact WILLARD D LARSON
Regulation Number878.4950
Classification Product Code
FWZ  
Date Received02/01/1989
Decision Date 02/10/1989
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
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