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Cellvizio 100 series system with confocal Miniprobes

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K220477
510(k) Type
Traditional
Applicant
Mauna Kea Technologies
Country
France
FDA Decision
Substantially Equivalent
Decision Date
4/11/2022
Days to Decision
52 days
Submission Type
Summary

Cellvizio 100 series system with confocal Miniprobes

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K220477
510(k) Type
Traditional
Applicant
Mauna Kea Technologies
Country
France
FDA Decision
Substantially Equivalent
Decision Date
4/11/2022
Days to Decision
52 days
Submission Type
Summary