Search Results
Found 1 results
510(k) Data Aggregation
K Number
K961358Manufacturer
Date Cleared
1996-07-02
(85 days)
Product Code
Regulation Number
870.3535Type
TraditionalPanel
CardiovascularReference & Predicate Devices
N/A
Why did this record match?
Device Name :
ARROW SHEATHLESS INTRA-AORTIC BALLOON 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
Page 1 of 1