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510(k) Data Aggregation
K Number
K965249Device Name
SPYGLASS ANGIOGRAPHIC CATHETERManufacturer
Date Cleared
1997-02-21
(71 days)
Product Code
Regulation Number
870.1200Type
TraditionalPanel
CardiovascularReference & Predicate Devices
N/A
Why did this record match?
Device Name :
SPYGLASS ANGIOGRAPHIC CATHETER
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
AI/ML Overview
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K Number
K962805Device Name
SPYGLASS ANGIOGRAPHIC CATHETERManufacturer
Date Cleared
1996-10-15
(89 days)
Product Code
Regulation Number
870.1200Type
TraditionalPanel
CardiovascularReference & Predicate Devices
N/A
Why did this record match?
Device Name :
SPYGLASS ANGIOGRAPHIC CATHETER
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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