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510(k) Data Aggregation
K Number
K002758Manufacturer
Date Cleared
2001-02-22
(170 days)
Product Code
Regulation Number
870.1025Type
TraditionalPanel
CardiovascularReference & Predicate Devices
N/A
Why did this record match?
Applicant Name (Manufacturer) :
AGILENT TECHNOLOGIES DEUTSCHLAND GMBH
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
AI/ML Overview
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K Number
K003038Manufacturer
Date Cleared
2000-12-15
(77 days)
Regulation Number
882.1400Type
TraditionalPanel
NeurologyReference & Predicate Devices
N/A
Why did this record match?
Applicant Name (Manufacturer) :
AGILENT TECHNOLOGIES DEUTSCHLAND GMBH
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
AI/ML Overview
Ask a Question
Ask a specific question about this device
K Number
K001722Manufacturer
Date Cleared
2000-06-30
(24 days)
Product Code
Regulation Number
870.1025Type
SpecialPanel
CardiovascularReference & Predicate Devices
N/A
Why did this record match?
Applicant Name (Manufacturer) :
AGILENT TECHNOLOGIES DEUTSCHLAND GMBH
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
AI/ML Overview
Ask a Question
Ask a specific question about this device
K Number
K001333Manufacturer
Date Cleared
2000-05-17
(20 days)
Product Code
Regulation Number
870.1025Type
SpecialPanel
CardiovascularReference & Predicate Devices
N/A
Why did this record match?
Applicant Name (Manufacturer) :
AGILENT TECHNOLOGIES DEUTSCHLAND GMBH
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
AI/ML Overview
Ask a Question
Ask a specific question about this device
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