Greenmedi Safety Filter Syringe
K-Number: K173743 · 2019-01-28
ApplicantSang-A Frontec Co., Ltd.
Decision Date2019-01-28
Product CodeMEG
Advisory CommitteeHO
DecisionSubstantially Equivalent
Device Summary
Greenmedi Safety Filter Syringe is a medical device manufactured by Sang-A Frontec Co., Ltd.. It received FDA 510(k) clearance on 2019-01-28 under approval number K173743. The device is classified under product code MEG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
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. It is manufactured by Sang-A Frontec Co., Ltd.. The 510(k) number is K173743.
When was Greenmedi Safety Filter Syringe approved by the FDA?
Greenmedi Safety Filter Syringe received FDA 510(k) clearance on 2019-01-28, under approval number K173743.
What company makes Greenmedi Safety Filter Syringe?
Greenmedi Safety Filter Syringe is manufactured by Sang-A Frontec Co., Ltd..
What is the FDA product code for Greenmedi Safety Filter Syringe?
The FDA product code for Greenmedi Safety Filter Syringe is MEG.
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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.