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510(k) Data Aggregation
K Number
K000901Manufacturer
Date Cleared
2000-07-05
(106 days)
Product Code
Regulation Number
878.4040Type
TraditionalPanel
General HospitalReference & Predicate Devices
N/A
Why did this record match?
Device Name :
KLINIDRAPE SURGICAL GOWNS, NON-REINFORCED, BASIC PROTECTIONS AND STANDARD PROTECTION
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use
Device Description
AI/ML Overview
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