Sterile Hypodermic Syringe for Single Use

FDA 510(k) K212207 · Shandong Weigao Group Medical Polymer Co., Ltd.

Substantially Equivalent

510(k) numberK212207

Submission

Device name
Sterile Hypodermic Syringe for Single Use
Applicant
Shandong Weigao Group Medical Polymer Co., Ltd.
Weihai, CN
Received
July 15, 2021
Decision date
March 23, 2023
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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More from Instylla, Inc.

510(k)DeviceDecision
K212920Sterile Safety Syringe with Needle for Single Use, Sterile Safety Hypodermic Needle for…FMF · Traditional 03/11/2022SE
K102741Enteral Feeding Bag and SetsKNT · Traditional 11/08/2011SE
K102328Blunt Fill Needle and Blunt Plastic CannulaFMI · Traditional 05/13/2011SE
K081241Weigao Empty Cartridge SyringeFMF · Traditional 09/08/2008SE
K072739Jierui Syringes and NeedlesMEG · Traditional 03/21/2008SE
K073127Blood Collection Needle, Model 20G 21G 22GFMI · Traditional 12/20/2007SE

Questions and answers

When was Sterile Hypodermic Syringe for Single Use cleared by the FDA?

Sterile Hypodermic Syringe for Single Use (K212207) received a 510(k) decision of Substantially Equivalent on March 23, 2023, 616 days after the submission was received.

What is the product code of K212207?

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