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510(k) Data Aggregation
K Number
K002906Manufacturer
Date Cleared
2000-12-15
(88 days)
Product Code
Regulation Number
N/AType
TraditionalReference & Predicate Devices
N/A
Why did this record match?
Device Name :
ULTRACISION HARMONIC SCALPEL SYSTEM, MODELS GEN01, GEN02, GEN03, HP052, HP053, HSA07
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
AI/ML Overview
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