Pen Injector
K-Number: K240774 · 2024-06-18
Device Summary
Frequently Asked Questions
What is the Pen Injector?
Pen Injector is a medical device that received FDA 510(k) clearance on 2024-06-18. The listed applicant is Wuxi Nest Biotechnology Co., Ltd.. The 510(k) number is K240774.
When did Pen Injector receive FDA 510(k) clearance?
Pen Injector received FDA 510(k) clearance on 2024-06-18, under 510(k) number K240774.
Who is the listed applicant for Pen Injector?
The FDA 510(k) record lists Wuxi Nest Biotechnology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Pen Injector?
The FDA product code for Pen Injector is FMF.
Other records listing Wuxi Nest Biotechnology Co., Ltd. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: FMF)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.