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510(k) Data Aggregation
K Number
K960738Manufacturer
Date Cleared
1997-05-06
(438 days)
Product Code
Regulation Number
880.6850Type
TraditionalPanel
General HospitalReference & Predicate Devices
N/A
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Device Name :
STERITITE SEALED CONTAINER(SC08F,SC06F,SC04F,SC08Q,SC06Q,SC04Q,SC08H,SC06H,SC04H)
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
AI/ML Overview
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