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FDA 510(k)

DJF Intravascular Administration Set

K-Number: K230992 · 2023-06-09

Decision Date2023-06-09
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DJF Intravascular Administration Set is the device name listed in this FDA 510(k) record. The listed applicant is Yangzhou Wei DE LI Trade Co., Ltd.. It received FDA 510(k) clearance on 2023-06-09 under 510(k) 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. The listed applicant is Yangzhou Wei DE LI Trade Co., Ltd.. The 510(k) number is K230992.

When did DJF Intravascular Administration Set receive FDA 510(k) clearance?

DJF Intravascular Administration Set received FDA 510(k) clearance on 2023-06-09, under 510(k) number K230992.

Who is the listed applicant for DJF Intravascular Administration Set?

The FDA 510(k) record lists Yangzhou Wei DE LI Trade Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DJF Intravascular Administration Set?

The FDA product code for DJF Intravascular Administration Set is FPA.

Related Devices (Code: FPA)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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