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EXPLORER AIR® II

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222240
510(k) Type
Traditional
Applicant
SurgVision GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
2/28/2023
Days to Decision
217 days
Submission Type
Summary

EXPLORER AIR® II

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222240
510(k) Type
Traditional
Applicant
SurgVision GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
2/28/2023
Days to Decision
217 days
Submission Type
Summary