Nipro Syringe
K-Number: K191359 · 2019-10-09
ApplicantNipro Medical Corporation
Decision Date2019-10-09
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent
Device Summary
Nipro Syringe is a medical device manufactured by Nipro Medical Corporation. It received FDA 510(k) clearance on 2019-10-09 under approval number K191359. 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 Nipro Syringe?
Nipro Syringe is a medical device that received FDA 510(k) clearance on 2019-10-09. It is manufactured by Nipro Medical Corporation. The 510(k) number is K191359.
When was Nipro Syringe approved by the FDA?
Nipro Syringe received FDA 510(k) clearance on 2019-10-09, under approval number K191359.
What company makes Nipro Syringe?
Nipro Syringe is manufactured by Nipro Medical Corporation.
What is the FDA product code for Nipro Syringe?
The FDA product code for Nipro Syringe is FMF.
Other Devices by Nipro Medical Corporation
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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.