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510(k) Data Aggregation
K Number
DEN240048Device Name
Spur Peripheral Retrievable Stent System
Manufacturer
Reflow Medical, Inc.
Date Cleared
2025-05-29
(251 days)
Product Code
SEU
Regulation Number
870.5110Why did this record match?
Product Code :
SEU
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
Intended Use
Device Description
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