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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Bottle, Collection, Vacuum
510(k) Number K770649
Device Name VAC-RITE
Applicant
MEDICAL DEVELOPMENT CO.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
MEDICAL DEVELOPMENT CO.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number880.6740
Classification Product Code
KDQ  
Date Received04/06/1977
Decision Date 06/02/1977
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
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