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XPERT 40 SPECIMEN RADIOGRAPHY SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K071233
510(k) Type
Traditional
Applicant
KUB TECHNOLOGIES, INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/20/2007
Days to Decision
48 days
Submission Type
Summary

XPERT 40 SPECIMEN RADIOGRAPHY SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K071233
510(k) Type
Traditional
Applicant
KUB TECHNOLOGIES, INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/20/2007
Days to Decision
48 days
Submission Type
Summary