Search Results
Found 1 results
510(k) Data Aggregation
K Number
K003442Device Name
MODIFICATION TO EDI VERIS SYSTEMManufacturer
Date Cleared
2001-05-04
(179 days)
Product Code
Regulation Number
886.1630Type
TraditionalPanel
Ophthalmic (OP)Reference & Predicate Devices
N/A
Why did this record match?
Device Name :
MODIFICATION TO EDI VERIS SYSTEM
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
Page 1 of 1