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510(k) Data Aggregation
K Number
K000355Manufacturer
Date Cleared
2000-08-23
(201 days)
Product Code
Regulation Number
880.2800Type
TraditionalPanel
General HospitalReference & Predicate Devices
N/A
Why did this record match?
Device Name :
3M COMPLY 1249 LIQUID PERACETIC ACID CHEMICAL INDICATOR
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
AI/ML Overview
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