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510(k) Data Aggregation
K Number
K002565Device Name
BAYLIS PAIN MANAGEMENT GENERATOR MODEL: PMG-115 (FOR DOMESTIC USE), PMG-230 (FOR INTERNATIONAL USE)Manufacturer
Date Cleared
2001-05-03
(259 days)
Product Code
Regulation Number
882.4400Type
TraditionalPanel
NeurologyReference & Predicate Devices
N/A
Predicate For
N/A
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
AI/ML Overview
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