DJF Intravascular Administration Set
K-Number: K230992 · 2023-06-09
ApplicantYangzhou Wei DE LI Trade Co., Ltd.
Decision Date2023-06-09
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent
Device Summary
DJF Intravascular Administration Set is a medical device manufactured by Yangzhou Wei DE LI Trade Co., Ltd.. It received FDA 510(k) clearance on 2023-06-09 under approval number K230992. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the DJF Intravascular Administration Set?
DJF Intravascular Administration Set is a medical device that received FDA 510(k) clearance on 2023-06-09. It is manufactured by Yangzhou Wei DE LI Trade Co., Ltd.. The 510(k) number is K230992.
When was DJF Intravascular Administration Set approved by the FDA?
DJF Intravascular Administration Set received FDA 510(k) clearance on 2023-06-09, under approval number K230992.
What company makes DJF Intravascular Administration Set?
DJF Intravascular Administration Set is manufactured by Yangzhou Wei DE LI Trade Co., Ltd..
What is the FDA product code for DJF Intravascular Administration Set?
The FDA product code for DJF Intravascular Administration Set is FPA.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.