C&B RESIN PLUS POWDER/LIQUID, MODELS RETEMP A2, A3, A3.5, CL, RETEMP B2, B3, C2, D3, WH, RETEMP MO— 510(k) K000894

Name: FDA 510(k) clearance K000894
Creator: U.S. Food and Drug Administration
Published: 2000-05-19

Substantially Equivalent

Dental Ventures of America, Inc.

FDA 510(k) clearance K000894 for C&B RESIN PLUS POWDER/LIQUID, MODELS RETEMP A2, A3, A3.5, CL, RETEMP B2, B3, C2, D3, WH, RETEMP MO, Substantially Equivalent on 2000-05-19. Applicant: Dental Ventures of America, Inc.. Device class: 2.

Clearance details

Applicant: Dental Ventures of America, Inc.
Product code: Code EBG
Device class: Class 2
Regulation: 21 CFR 872.3770
Advisory panel: Dental
Date received: 2000-03-20
Decision date: 2000-05-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Corona, CA, US

Download summary PDF View on FDA.gov ↗

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