Last synced on 12 July 2024 at 11:04 pm

K Clear

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K220726
510(k) Type
Traditional
Applicant
K Line Europe GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
3/16/2022
Days to Decision
2 days
Submission Type
Summary

K Clear

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K220726
510(k) Type
Traditional
Applicant
K Line Europe GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
3/16/2022
Days to Decision
2 days
Submission Type
Summary