Search Results
Found 1 results
510(k) Data Aggregation
K Number
K003349Device Name
ALLON 2001 MODIFIEDManufacturer
Date Cleared
2000-11-13
(18 days)
Product Code
Regulation Number
870.5900Type
SpecialPanel
CardiovascularReference & Predicate Devices
N/A
Why did this record match?
Device Name :
ALLON 2001 MODIFIED
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
Page 1 of 1