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REMESENSE FOR SENSITIVE TEETH

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K122708
510(k) Type
Traditional
Applicant
SYLPHAR N.V.
Country
Italy
FDA Decision
Substantially Equivalent
Decision Date
1/14/2013
Days to Decision
132 days
Submission Type
Summary

REMESENSE FOR SENSITIVE TEETH

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K122708
510(k) Type
Traditional
Applicant
SYLPHAR N.V.
Country
Italy
FDA Decision
Substantially Equivalent
Decision Date
1/14/2013
Days to Decision
132 days
Submission Type
Summary