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510(k) Data Aggregation
K Number
K953452Device Name
KETOREX C SANWA
Manufacturer
Date Cleared
1996-05-02
(289 days)
Product Code
Regulation Number
862.1380Why did this record match?
Applicant Name (Manufacturer) :
IHARA MEDICS U.S., INC.
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
Intended Use
Device Description
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