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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Clamp, Line
510(k) Number K844121
Device Name CLAMP, TUBING, LINE
Applicant
Dyn-A-Med Products
255 Bluff Ct.
Barrington,  IL  60010
Applicant Contact RICHARD J VANNOTE
Correspondent
Dyn-A-Med Products
255 Bluff Ct.
Barrington,  IL  60010
Correspondent Contact RICHARD J VANNOTE
Regulation Number876.4730
Classification Product Code
FKK  
Date Received10/23/1984
Decision Date 12/17/1984
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Gastroenterology/Urology
510k Review Panel Gastroenterology/Urology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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