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CARIESCAN PRO

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K090598
510(k) Type
Traditional
Applicant
CARIESCAN LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
12/15/2009
Days to Decision
285 days
Submission Type
Summary

CARIESCAN PRO

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K090598
510(k) Type
Traditional
Applicant
CARIESCAN LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
12/15/2009
Days to Decision
285 days
Submission Type
Summary