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DENTIMAX DIGITAL X-RAY IMAGING SYSTEM SENSOR SIZE 1, 2, DENTIMAX USB CONTROL BOX

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092547
510(k) Type
Traditional
Applicant
DENTIMAX
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/30/2009
Days to Decision
72 days
Submission Type
Summary

DENTIMAX DIGITAL X-RAY IMAGING SYSTEM SENSOR SIZE 1, 2, DENTIMAX USB CONTROL BOX

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092547
510(k) Type
Traditional
Applicant
DENTIMAX
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/30/2009
Days to Decision
72 days
Submission Type
Summary