Last synced on 25 January 2026 at 3:41 am

MolecuLight I:X

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213840
510(k) Type
Traditional
Applicant
Moleculight, Inc.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
5/18/2022
Days to Decision
160 days
Submission Type
Summary

MolecuLight I:X

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213840
510(k) Type
Traditional
Applicant
Moleculight, Inc.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
5/18/2022
Days to Decision
160 days
Submission Type
Summary