Insulin Syringes without needle

FDA 510(k) K221045 · Berpu Medical Technology Co., Ltd.

Substantially Equivalent

510(k) numberK221045

Submission

Device name
Insulin Syringes without needle
Applicant
Berpu Medical Technology Co., Ltd.
Wenzhou, CN
Received
April 8, 2022
Decision date
November 3, 2022
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

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

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K253112Sofjec (Single use Needle); Sofjec (Single use Syringe with or without Needle); Sofjec…FMF · Special Hlb Lifescience Co., Ltd.05/21/2026SE
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More from Instylla, Inc.

510(k)DeviceDecision
K232165Sterile Safety Hypodermic Needles for Single Use; Sterile Hypodermic Needles for Single…FMI · Traditional 02/01/2024SE
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
K180417Self-destruction Safety Syringes for Single Use; Sterile Hypodermic Syringes for Single…MEG · Traditional 08/09/2018SE
K162180Disposable Insulin SyringeFMF · Traditional 12/29/2016SE

Questions and answers

When was Insulin Syringes without needle cleared by the FDA?

Insulin Syringes without needle (K221045) received a 510(k) decision of Substantially Equivalent on November 3, 2022, 209 days after the submission was received.

What is the product code of K221045?

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