Last synced on 25 April 2025 at 11:05 pm

CRANIAL STEREOTACTIC EQUIPMENT

Page Type
Cleared 510(K)
PDF
FDA Hosted 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
FDA Hosted 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