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510(k) Data Aggregation
K Number
K001994Device Name
EEI SLUSH PAN DRAPEManufacturer
Date Cleared
2000-08-04
(35 days)
Product Code
Regulation Number
878.4370Type
TraditionalPanel
General HospitalReference & Predicate Devices
N/A
Predicate For
N/A
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
AI/ML Overview
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K Number
K001264Device Name
EAGLE ENDO SPECIMEN RETRIEVAL BAGManufacturer
Date Cleared
2000-05-30
(41 days)
Product Code
Regulation Number
876.1500Type
TraditionalReference & Predicate Devices
N/A
Predicate For
N/A
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
AI/ML Overview
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Ask a specific question about this device
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