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510(k) Data Aggregation
K Number
K002389Device Name
BAYLIS PAIN MANAGEMENT PROBE/PMP-20-145 AND BAYLIS PAIN MANAGEMENT CONNECTOR CABLE/PMX-BAY-BAYManufacturer
Date Cleared
2000-10-23
(80 days)
Product Code
Regulation Number
882.4725Type
TraditionalPanel
NeurologyReference & Predicate Devices
N/A
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Device Name :
BAYLIS PAIN MANAGEMENT PROBE/PMP-20-145 AND BAYLIS PAIN MANAGEMENT CONNECTOR CABLE/PMX-BAY-BAY
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
AI/ML Overview
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