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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Clamp, Tubing, Blood, Automatic
510(k) Number K914459
Device Name AUTOMATIC TUBING CLAMP
Applicant
Rocky Mountain Research, Inc.
2715 E. 3300 S.
Salt Lake City,  UT  84109
Applicant Contact THERESE DAVY
Correspondent
Rocky Mountain Research, Inc.
2715 E. 3300 S.
Salt Lake City,  UT  84109
Correspondent Contact THERESE DAVY
Regulation Number876.5820
Classification Product Code
FIG  
Date Received10/07/1991
Decision Date 06/24/1992
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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