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ADPHARMA OCCLUDE AND OCCLUDE F DENTIN TUBULE AGENT

Page Type
Cleared 510(K)
510(k) Number
K082071
510(k) Type
Traditional
Applicant
Adpharma, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/2/2008
Days to Decision
72 days
Submission Type
Summary

ADPHARMA OCCLUDE AND OCCLUDE F DENTIN TUBULE AGENT

Page Type
Cleared 510(K)
510(k) Number
K082071
510(k) Type
Traditional
Applicant
Adpharma, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/2/2008
Days to Decision
72 days
Submission Type
Summary