Last synced on 25 January 2026 at 3:41 am

C&B RESIN PLUS POWDER/LIQUID, MODELS RETEMP A2, A3, A3.5, CL, RETEMP B2, B3, C2, D3, WH, RETEMP MO

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K000894
510(k) Type
Traditional
Applicant
Dental Ventures of America, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/19/2000
Days to Decision
60 days
Submission Type
Statement

C&B RESIN PLUS POWDER/LIQUID, MODELS RETEMP A2, A3, A3.5, CL, RETEMP B2, B3, C2, D3, WH, RETEMP MO

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K000894
510(k) Type
Traditional
Applicant
Dental Ventures of America, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/19/2000
Days to Decision
60 days
Submission Type
Statement