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510(k) Data Aggregation
K Number
K001776Manufacturer
Date Cleared
2000-06-30
(30 days)
Product Code
Regulation Number
870.2300Type
SpecialPanel
CardiovascularReference & Predicate Devices
N/A
Why did this record match?
Device Name :
MODIFICATION TO HP M2376A DEVICE LINK SYSTEM, MODEL M2376A
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
AI/ML Overview
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K Number
K000635Device Name
MODIFICATION TO HP M2376A DEVICE LINK SYSTEMManufacturer
Date Cleared
2000-03-20
(24 days)
Product Code
Regulation Number
870.2300Type
SpecialPanel
CardiovascularReference & Predicate Devices
N/A
Why did this record match?
Device Name :
MODIFICATION TO HP M2376A DEVICE LINK SYSTEM
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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