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510(k) Data Aggregation
K Number
K954999Device Name
LILY MULTICANNULA GUIDE
Manufacturer
Date Cleared
1996-04-04
(155 days)
Product Code
Regulation Number
876.1075Why did this record match?
Applicant Name (Manufacturer) :
LILY IMAGING SOLUTIONS CO.
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
Intended Use
Device Description
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K Number
K954998Device Name
LILY DARK VIEWER
Manufacturer
Date Cleared
1996-01-29
(89 days)
Product Code
Regulation Number
892.1890Why did this record match?
Applicant Name (Manufacturer) :
LILY IMAGING SOLUTIONS CO.
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
Intended Use
Device Description
Ask a Question
Ask a specific question about this device
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