Sterile Hypodermic Syringes for Single Use
K-Number: K221079 · 2022-10-04
Device Summary
Frequently Asked Questions
What is the Sterile Hypodermic Syringes for Single Use?
Sterile Hypodermic Syringes for Single Use is a medical device that received FDA 510(k) clearance on 2022-10-04. It is manufactured by Sichuan Prius Biotechnology Co., Ltd.. The 510(k) number is K221079.
When was Sterile Hypodermic Syringes for Single Use approved by the FDA?
Sterile Hypodermic Syringes for Single Use received FDA 510(k) clearance on 2022-10-04, under approval number K221079.
What company makes Sterile Hypodermic Syringes for Single Use?
Sterile Hypodermic Syringes for Single Use is manufactured by Sichuan Prius Biotechnology Co., Ltd..
What is the FDA product code for Sterile Hypodermic Syringes for Single Use?
The FDA product code for Sterile Hypodermic Syringes for Single Use is FMF.
Related Clinical Trials
Related PubMed Literature
Other Devices by Sichuan Prius Biotechnology Co., Ltd.
Related Devices (Code: FMF)
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.