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510(k) Data Aggregation
K Number
K961782Device Name
BIO-BINKI
Manufacturer
Date Cleared
1997-03-28
(324 days)
Product Code
Regulation Number
892.1650Why did this record match?
Applicant Name (Manufacturer) :
BIOMNI MEDICAL SYSTEMS, INC.
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
Intended Use
Device Description
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