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510(k) Data Aggregation
K Number
K960426Manufacturer
Date Cleared
1996-03-21
(52 days)
Product Code
Regulation Number
878.4200Type
TraditionalReference & Predicate Devices
N/A
Why did this record match?
Device Name :
MEDICOMP FLEXI-SMOOTH WOUND DRAINAGE CATHETER
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
AI/ML Overview
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