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CROSSPLAN / ACCUSOFT-XL V.4.04

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K063482
510(k) Type
Special
Applicant
Direx Systems Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/14/2006
Days to Decision
27 days
Submission Type
Summary

CROSSPLAN / ACCUSOFT-XL V.4.04

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K063482
510(k) Type
Special
Applicant
Direx Systems Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/14/2006
Days to Decision
27 days
Submission Type
Summary