Greenmedi Safety Filter Syringe
K-Number: K173743 · 2019-01-28
Device Summary
Frequently Asked Questions
What is the Greenmedi Safety Filter Syringe?
Greenmedi Safety Filter Syringe is a medical device that received FDA 510(k) clearance on 2019-01-28. The listed applicant is Sang-A Frontec Co., Ltd.. The 510(k) number is K173743.
When did Greenmedi Safety Filter Syringe receive FDA 510(k) clearance?
Greenmedi Safety Filter Syringe received FDA 510(k) clearance on 2019-01-28, under 510(k) number K173743.
Who is the listed applicant for Greenmedi Safety Filter Syringe?
The FDA 510(k) record lists Sang-A Frontec Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Greenmedi Safety Filter Syringe?
The FDA product code for Greenmedi Safety Filter Syringe is MEG.
Related Devices (Code: MEG)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
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