Shoocin Introducer Kit
K-Number: K172099 · 2017-10-05
Decision Date2017-10-05
Product CodeDYB
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
Shoocin Introducer Kit is a medical device manufactured by Lepu Medical Technology (Beijing) Co., Ltd.. It received FDA 510(k) clearance on 2017-10-05 under approval number K172099. The device is classified under product code DYB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
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. It is manufactured by Lepu Medical Technology (Beijing) Co., Ltd.. The 510(k) number is K172099.
When was Shoocin Introducer Kit approved by the FDA?
Shoocin Introducer Kit received FDA 510(k) clearance on 2017-10-05, under approval number K172099.
What company makes Shoocin Introducer Kit?
Shoocin Introducer Kit is manufactured by Lepu Medical Technology (Beijing) Co., Ltd..
What is the FDA product code for Shoocin Introducer Kit?
The FDA product code for Shoocin Introducer Kit is DYB.
Other Devices by Lepu Medical Technology (Beijing) 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.