Search Results
Found 1 results
510(k) Data Aggregation
K Number
K004006Manufacturer
Date Cleared
2001-03-26
(90 days)
Product Code
Regulation Number
878.4810Type
TraditionalReference & Predicate Devices
N/A
Why did this record match?
Device Name :
SELECTA 7000 FREQUENCY DOUBLED, Q-SWITCHED ND:YAG OPHTHALMIC LASER
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