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CRANIAL STEREOTACTIC EQUIPMENT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K010065
510(k) Type
Traditional
Applicant
Arplay Medical S.A.
Country
France
FDA Decision
Substantially Equivalent
Decision Date
7/2/2002
Days to Decision
540 days
Submission Type
Summary

CRANIAL STEREOTACTIC EQUIPMENT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K010065
510(k) Type
Traditional
Applicant
Arplay Medical S.A.
Country
France
FDA Decision
Substantially Equivalent
Decision Date
7/2/2002
Days to Decision
540 days
Submission Type
Summary