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510(k) Data Aggregation
K Number
K003239Manufacturer
Date Cleared
2000-11-30
(44 days)
Product Code
Regulation Number
862.1660Type
TraditionalReference & Predicate Devices
N/A
Why did this record match?
Device Name :
LIQUICHEK BLOOD GAS PLUS CO-OXIMETER CONTROL (800 SERIES), MODEL504,505,506
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
AI/ML Overview
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