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ACCUSOFT, ACCUSOFT XL

Page Type
Cleared 510(K)
510(k) Number
K062032
510(k) Type
Traditional
Applicant
DIREX SYSTEMS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/5/2006
Days to Decision
79 days
Submission Type
Summary

ACCUSOFT, ACCUSOFT XL

Page Type
Cleared 510(K)
510(k) Number
K062032
510(k) Type
Traditional
Applicant
DIREX SYSTEMS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/5/2006
Days to Decision
79 days
Submission Type
Summary