Last synced on 14 June 2024 at 11:05 pm

CROSSPLAN / ACCUSOFT-XL V.4.04

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