Oral/Enteral Syringe
K-Number: K210621 · 2021-04-28
Decision Date2021-04-28
Product CodePNR
Advisory CommitteeGU
DecisionSubstantially Equivalent
Device Summary
Oral/Enteral Syringe is a medical device manufactured by Ningbo Tianyi Medical Appliance Co., Ltd.. It received FDA 510(k) clearance on 2021-04-28 under approval number K210621. The device is classified under product code PNR. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Oral/Enteral Syringe?
Oral/Enteral Syringe is a medical device that received FDA 510(k) clearance on 2021-04-28. It is manufactured by Ningbo Tianyi Medical Appliance Co., Ltd.. The 510(k) number is K210621.
When was Oral/Enteral Syringe approved by the FDA?
Oral/Enteral Syringe received FDA 510(k) clearance on 2021-04-28, under approval number K210621.
What company makes Oral/Enteral Syringe?
Oral/Enteral Syringe is manufactured by Ningbo Tianyi Medical Appliance Co., Ltd..
What is the FDA product code for Oral/Enteral Syringe?
The FDA product code for Oral/Enteral Syringe is PNR.
Other Devices by Ningbo Tianyi Medical Appliance Co., Ltd.
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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.