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510(k) Data Aggregation
K Number
K090210Manufacturer
Date Cleared
2009-07-29
(182 days)
Product Code
Regulation Number
876.1300Type
SpecialReference & Predicate Devices
N/A
Why did this record match?
Device Name :
MODIFICATION TO OLYMPUS CAPSULE ENDOSCOPE SYSTEM
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
AI/ML Overview
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