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510(k) Data Aggregation
K Number
K002044Device Name
MAGNA FORTIS OPHTHALMOSCOPE DIAGNOSTIC KIT
Manufacturer
Date Cleared
2000-09-12
(69 days)
Regulation Number
886.1570Why did this record match?
Applicant Name (Manufacturer) :
MAGNA FORTIS CORPORATION
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
Intended Use
Device Description
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