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BOND-IT DUAL CURE ACTIVATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K953859
510(k) Type
Traditional
Applicant
JENERIC/PENTRON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/7/1995
Days to Decision
21 days
Submission Type
Statement

BOND-IT DUAL CURE ACTIVATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K953859
510(k) Type
Traditional
Applicant
JENERIC/PENTRON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/7/1995
Days to Decision
21 days
Submission Type
Statement