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EXPLORER AIR® II (8001, 8002, 8003); EXPLORER AIR® Sterile Drape (8004)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K234090
510(k) Type
Traditional
Applicant
SurgVision GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
3/20/2024
Days to Decision
89 days
Submission Type
Summary

EXPLORER AIR® II (8001, 8002, 8003); EXPLORER AIR® Sterile Drape (8004)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K234090
510(k) Type
Traditional
Applicant
SurgVision GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
3/20/2024
Days to Decision
89 days
Submission Type
Summary