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510(k) Data Aggregation
K Number
K001962Manufacturer
Date Cleared
2001-07-09
(377 days)
Product Code
Regulation Number
886.5925Type
TraditionalPanel
OphthalmicReference & Predicate Devices
N/A
Why did this record match?
Applicant Name (Manufacturer) :
BESCON CO., LTD.
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
AI/ML Overview
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K Number
K002099Manufacturer
Date Cleared
2001-07-09
(363 days)
Product Code
Regulation Number
886.5925Type
TraditionalPanel
OphthalmicReference & Predicate Devices
N/A
Why did this record match?
Applicant Name (Manufacturer) :
BESCON CO., LTD.
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
AI/ML Overview
Ask a Question
Ask a specific question about this device
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