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510(k) Data Aggregation
K Number
K091855Manufacturer
Date Cleared
2009-07-01
(8 days)
Product Code
Regulation Number
880.5725Type
SpecialPanel
General HospitalReference & Predicate Devices
N/A
Why did this record match?
Device Name :
THE BELMONT FLUID MANAGEMENT SYSTEM/ THE BELMONT RAPID INFUSER, MODEL FMS2000
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
AI/ML Overview
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