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510(k) Data Aggregation
K Number
K963564Manufacturer
Date Cleared
1996-11-22
(78 days)
Product Code
Regulation Number
880.6760Type
TraditionalPanel
General HospitalReference & Predicate Devices
N/A
Why did this record match?
Device Name :
PERSONAL LIMB HOLDER (24444-200,300,24444-KIT)
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
AI/ML Overview
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