Last synced on 14 November 2025 at 11:06 pm

CoreLevee

Page Type
Cleared 510(K)
510(k) Number
K213748
510(k) Type
Traditional
Applicant
Lutronic Corporation
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
10/14/2022
Days to Decision
318 days
Submission Type
Summary

CoreLevee

Page Type
Cleared 510(K)
510(k) Number
K213748
510(k) Type
Traditional
Applicant
Lutronic Corporation
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
10/14/2022
Days to Decision
318 days
Submission Type
Summary