Pen Injector
K-Number: K240774 · 2024-06-18
ApplicantWuxi Nest Biotechnology Co., Ltd.
Decision Date2024-06-18
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent
Device Summary
Pen Injector is a medical device manufactured by Wuxi Nest Biotechnology Co., Ltd.. It received FDA 510(k) clearance on 2024-06-18 under approval number K240774. 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 Pen Injector?
Pen Injector is a medical device that received FDA 510(k) clearance on 2024-06-18. It is manufactured by Wuxi Nest Biotechnology Co., Ltd.. The 510(k) number is K240774.
When was Pen Injector approved by the FDA?
Pen Injector received FDA 510(k) clearance on 2024-06-18, under approval number K240774.
What company makes Pen Injector?
Pen Injector is manufactured by Wuxi Nest Biotechnology Co., Ltd..
What is the FDA product code for Pen Injector?
The FDA product code for Pen Injector is FMF.
Other Devices by Wuxi Nest Biotechnology 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.