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510(k) Data Aggregation
K Number
K002789Device Name
MEDEVIEW SYSTEM
Manufacturer
Date Cleared
2001-03-21
(195 days)
Product Code
Regulation Number
892.2050Why did this record match?
Applicant Name (Manufacturer) :
MEDEVIEW.COM
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
Intended Use
Device Description
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