Disposable Sterile Syringe, with/without needle;luer/luer-lock, Disposable insulin syringe, Disposable Hypodermic needle

FDA 510(k) K212033 · Shandong Zhushi Pharmaceutical Group Co., Ltd.

Substantially Equivalent

510(k) numberK212033

Submission

Device name
Disposable Sterile Syringe, with/without needle;luer/luer-lock, Disposable insulin syringe, Disposable Hypodermic needle
Applicant
Shandong Zhushi Pharmaceutical Group Co., Ltd.
Heze, CN
Received
June 29, 2021
Decision date
August 17, 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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Questions and answers

When was Disposable Sterile Syringe, with/without needle;luer/luer-lock, Disposable insulin syringe, Disposable Hypodermic needle cleared by the FDA?

Disposable Sterile Syringe, with/without needle;luer/luer-lock, Disposable insulin syringe, Disposable Hypodermic needle (K212033) received a 510(k) decision of Substantially Equivalent on August 17, 2022, 414 days after the submission was received.

What is the product code of K212033?

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