Sterile Single-use Infusion Set

FDA 510(k) K163160 · Jiangxi Hongda Medical Equipment Group , Ltd.

Substantially Equivalent

510(k) numberK163160

Submission

Device name
Sterile Single-use Infusion Set
Applicant
Jiangxi Hongda Medical Equipment Group , Ltd.
Nanchang, CN
Received
November 10, 2016
Decision date
April 20, 2017
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FPA – Set, Administration, Intravascular
Device class
Class II (moderate risk)
Regulation
21 CFR 880.5440
Specialty
General Hospital

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More from B.Braun Medical, Inc.

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K210578Medical Nitrile Examination Gloves (Power free, Blue)LZA · Traditional 07/10/2021SE
K210821Medical PVC Examination GlovesLYZ · Traditional 07/09/2021SE
K163162Sterile Hypodermic Safety Syringes for Single UseMEG · Traditional 03/20/2017SE
K163161Sterile Single-use Syringe with NeedleFMF · Traditional 03/20/2017SE

Questions and answers

When was Sterile Single-use Infusion Set cleared by the FDA?

Sterile Single-use Infusion Set (K163160) received a 510(k) decision of Substantially Equivalent on April 20, 2017, 161 days after the submission was received.

What is the product code of K163160?

The FDA product code is FPA – Set, Administration, Intravascular, a Class II (moderate risk) device regulated under 21 CFR 880.5440.