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510(k) Data Aggregation
K Number
K003352Device Name
ESCREEN SYSTEM
Manufacturer
Date Cleared
2001-03-20
(145 days)
Regulation Number
862.3610Why did this record match?
Applicant Name (Manufacturer) :
ESCREEN, INC.
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
Intended Use
Device Description
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