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510(k) Data Aggregation
K Number
K010802Device Name
CARDIAC VIEW, MODEL 2001
Manufacturer
Date Cleared
2001-06-08
(84 days)
Product Code
Regulation Number
892.1000Why did this record match?
Applicant Name (Manufacturer) :
MAGNA LAB, INC.
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
Intended Use
Device Description
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