Self-destruction Safety Syringes for Single Use; Sterile Hypodermic Syringes for Single Use; Sterile Hypodermic Needles for Single Use; Sterile Safety Hypodermic Needles for Single Use

FDA 510(k) K180417 · Berpu Medical Technology Co., Ltd.

Substantially Equivalent

510(k) numberK180417

Submission

Device name
Self-destruction Safety Syringes for Single Use; Sterile Hypodermic Syringes for Single Use; Sterile Hypodermic Needles for Single Use; Sterile Safety Hypodermic Needles for Single Use
Applicant
Berpu Medical Technology Co., Ltd.
Wenzhou, CN
Received
February 15, 2018
Decision date
August 9, 2018
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
MEG – Syringe, Antistick
Device class
Class II (moderate risk)
Regulation
21 CFR 880.5860
Specialty
General Hospital

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More from Jiangsu Kangbao Medical Equipment Co., Ltd.

510(k)DeviceDecision
K232165Sterile Safety Hypodermic Needles for Single Use; Sterile Hypodermic Needles for Single…FMI · Traditional 02/01/2024SE
K221045Insulin Syringes without needleFMF · Traditional 11/03/2022SE
K220061Safety Insulin SyringesMEG · Traditional 08/23/2022SE
K213158Syringe with permanently attached needleFMF · Traditional 07/21/2022SE
K213811Sterile Hypodermic Syringes for Single UseFMF · Traditional 05/12/2022SE
K212514Safety Pen Needle for Single Use, Insulin Pen NeedlesFMI · Traditional 04/29/2022SE
K181447Safety insulin needle for single useFMI · Traditional 03/12/2019SE
K162180Disposable Insulin SyringeFMF · Traditional 12/29/2016SE

Questions and answers

When was Self-destruction Safety Syringes for Single Use; Sterile Hypodermic Syringes for Single Use; Sterile Hypodermic Needles for Single Use; Sterile Safety Hypodermic Needles for Single Use cleared by the FDA?

Self-destruction Safety Syringes for Single Use; Sterile Hypodermic Syringes for Single Use; Sterile Hypodermic Needles for Single Use; Sterile Safety Hypodermic Needles for Single Use (K180417) received a 510(k) decision of Substantially Equivalent on August 9, 2018, 175 days after the submission was received.

What is the product code of K180417?

The FDA product code is MEG – Syringe, Antistick, a Class II (moderate risk) device regulated under 21 CFR 880.5860.