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510(k) Data Aggregation
K Number
K001146Device Name
GENYX FLEXIBLE INJECTION NEEEDLE
Manufacturer
Date Cleared
2000-06-30
(81 days)
Product Code
Regulation Number
876.1500Why did this record match?
Applicant Name (Manufacturer) :
GENY MEDICAL, INC.
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
Intended Use
Device Description
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