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EOlife®

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221841
510(k) Type
Traditional
Applicant
ARCHEON
Country
France
FDA Decision
Substantially Equivalent
Decision Date
3/18/2023
Days to Decision
267 days
Submission Type
Summary

EOlife®

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221841
510(k) Type
Traditional
Applicant
ARCHEON
Country
France
FDA Decision
Substantially Equivalent
Decision Date
3/18/2023
Days to Decision
267 days
Submission Type
Summary