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GENERATION 8 SE ADHESIVE

Page Type
Cleared 510(K)
510(k) Number
K072480
510(k) Type
Traditional
Applicant
PENTRON CLINICAL TECHNOLOGIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/21/2007
Days to Decision
78 days
Submission Type
Summary

GENERATION 8 SE ADHESIVE

Page Type
Cleared 510(K)
510(k) Number
K072480
510(k) Type
Traditional
Applicant
PENTRON CLINICAL TECHNOLOGIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/21/2007
Days to Decision
78 days
Submission Type
Summary