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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 K770510
Device Name CANNULA, INTRAVENOUS, TEFLON
Applicant
Sherwood Medical Industries
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Sherwood Medical Industries
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number880.5200
Classification Product Code
FOZ  
Date Received03/17/1977
Decision Date 05/10/1977
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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