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510(k) Data Aggregation
K Number
K193005Device Name
DIMI RRT System
Manufacturer
Date Cleared
2020-08-28
(305 days)
Product Code
Regulation Number
876.5860Why did this record match?
Applicant Name (Manufacturer) :
Dialco Medical Inc.
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
Intended Use
for the indications for use stated in the enclosure
Device Description
Not Found
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