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510(k) Data Aggregation
K Number
K252524Device Name
Quadsense (Quadsense and Quadsense Pro)Manufacturer
Date Cleared
2025-09-09
(29 days)
Product Code
Regulation Number
882.4560Type
SpecialPanel
Orthopedic (OR)Reference & Predicate Devices
N/A
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Device Name :
Quadsense (Quadsense and Quadsense Pro)
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
AI/ML Overview
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