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Arkligners

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K220835
510(k) Type
Traditional
Applicant
Arklign Laboratories
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/12/2022
Days to Decision
143 days
Submission Type
Summary

Arkligners

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K220835
510(k) Type
Traditional
Applicant
Arklign Laboratories
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/12/2022
Days to Decision
143 days
Submission Type
Summary