Laport
K-Number: K171741 · 2017-08-29
ApplicantSejong Medical Co., Ltd.
Decision Date2017-08-29
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent
Device Summary
Laport is a medical device manufactured by Sejong Medical Co., Ltd.. It received FDA 510(k) clearance on 2017-08-29 under approval number K171741. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Laport?
Laport is a medical device that received FDA 510(k) clearance on 2017-08-29. It is manufactured by Sejong Medical Co., Ltd.. The 510(k) number is K171741.
When was Laport approved by the FDA?
Laport received FDA 510(k) clearance on 2017-08-29, under approval number K171741.
What company makes Laport?
Laport is manufactured by Sejong Medical Co., Ltd..
What is the FDA product code for Laport?
The FDA product code for Laport is GCJ.
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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.