WTF Secura Syringe and Needle

FDA 510(k) K132120 · Beijing Wantefu Medical Apparatus Co., Ltd.

Substantially Equivalent

510(k) numberK132120

Submission

Device name
WTF Secura Syringe and Needle
Applicant
Beijing Wantefu Medical Apparatus Co., Ltd.
Beijing, CN
Received
July 9, 2013
Decision date
December 12, 2013
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 WTF Secura Syringe and Needle cleared by the FDA?

WTF Secura Syringe and Needle (K132120) received a 510(k) decision of Substantially Equivalent on December 12, 2013, 156 days after the submission was received.

What is the product code of K132120?

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