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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Monitor, Esophageal Motility, Anorectal Motility, And Tube
510(k) Number K821588
Device Name SANDHILL DMS
Applicant
Sandhill
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Sandhill
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number876.1725
Classification Product Code
KLA  
Date Received06/01/1982
Decision Date 06/22/1982
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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