Shoocin Introducer Kit
K-Number: K172099 · 2017-10-05
Device Summary
Frequently Asked Questions
What is the Shoocin Introducer Kit?
Shoocin Introducer Kit is a medical device that received FDA 510(k) clearance on 2017-10-05. The listed applicant is Lepu Medical Technology (Beijing) Co., Ltd.. The 510(k) number is K172099.
When did Shoocin Introducer Kit receive FDA 510(k) clearance?
Shoocin Introducer Kit received FDA 510(k) clearance on 2017-10-05, under 510(k) number K172099.
Who is the listed applicant for Shoocin Introducer Kit?
The FDA 510(k) record lists Lepu Medical Technology (Beijing) Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Shoocin Introducer Kit?
The FDA product code for Shoocin Introducer Kit is DYB.
Other records listing Lepu Medical Technology (Beijing) 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: DYB)
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.