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PERMALUTE COMPOSITE LUTING/RESTORATIVE RESIN SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K960696
510(k) Type
Traditional
Applicant
ULTRADENT PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/18/1996
Days to Decision
149 days
Submission Type
Statement

PERMALUTE COMPOSITE LUTING/RESTORATIVE RESIN SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K960696
510(k) Type
Traditional
Applicant
ULTRADENT PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/18/1996
Days to Decision
149 days
Submission Type
Statement