Merit Syringe
K-Number: K171362 · 2017-08-07
ApplicantMerit Medical Systems, Inc.
Decision Date2017-08-07
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent
Device Summary
Merit Syringe is a medical device manufactured by Merit Medical Systems, Inc.. It received FDA 510(k) clearance on 2017-08-07 under approval number K171362. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Merit Syringe?
Merit Syringe is a medical device that received FDA 510(k) clearance on 2017-08-07. It is manufactured by Merit Medical Systems, Inc.. The 510(k) number is K171362.
When was Merit Syringe approved by the FDA?
Merit Syringe received FDA 510(k) clearance on 2017-08-07, under approval number K171362.
What company makes Merit Syringe?
Merit Syringe is manufactured by Merit Medical Systems, Inc..
What is the FDA product code for Merit Syringe?
The FDA product code for Merit Syringe is FMF.
Other Devices by Merit Medical Systems, Inc.
Related Devices (Code: FMF)
K162180Disposable Insulin SyringeBerpu Medical Technology Co., Ltd.
K162081BD 1ml Luer-lok Hypodermic Syringe, BD 1 mL Luer-Lok Hypodermic Syringe with BD Hypodermic Needle or BD Eclipse Hypodermic Needle, BD 1ml Luer-lok Insulin SyringeBecton, Dickinson and Company
K162602NovoPen EchoNovo Nordisk, Inc.
K161568Bone Solutions Mixing and Delivery SystemBone Solutions, Inc.
K152879Sure-Fine Insulin SyringesShina Med Corporation
K160629InPenCompanion Medical, Inc.
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.