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Laport

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K171741
510(k) Type
Traditional
Applicant
Sejong Medical Co., Ltd.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
8/29/2017
Days to Decision
78 days
Submission Type
Summary