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510(k) Data Aggregation
K Number
K162951Device Name
TUBETECH IV Administration Set
Manufacturer
Date Cleared
2017-07-28
(277 days)
Product Code
Regulation Number
880.5440Why did this record match?
Applicant Name (Manufacturer) :
Douglas Medical Products, Inc.
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
Intended Use
For the administration of fluids from a container into the patient vascular system through a vascular access device.
Device Description
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