SANDHILL DMS

Monitor, Esophageal Motility, And Tube

SANDHILL

The following data is part of a premarket notification filed by Sandhill with the FDA for Sandhill Dms.

Pre-market Notification Details

Device IDK821588
510k NumberK821588
Device Name:SANDHILL DMS
ClassificationMonitor, Esophageal Motility, And Tube
Applicant SANDHILL 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeKLA  
CFR Regulation Number876.1725 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1982-06-01
Decision Date1982-06-22

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