DREAM BOND, DREAMCAST CHROME, DREAMCAST V, DREAM FLEXICAST, DREAM LITHECAST— 510(k) K033045

Name: FDA 510(k) clearance K033045
Creator: U.S. Food and Drug Administration
Published: 2003-12-23

Substantially Equivalent

American Green Dent. Mfg, Inc.

FDA 510(k) clearance K033045 for DREAM BOND, DREAMCAST CHROME, DREAMCAST V, DREAM FLEXICAST, DREAM LITHECAST, Substantially Equivalent on 2003-12-23. Applicant: American Green Dent. Mfg, Inc.. Device class: 2.

Clearance details

Applicant: American Green Dent. Mfg, Inc.
Product code: Code EJH
Device class: Class 2
Regulation: 21 CFR 872.3710
Advisory panel: Dental
Date received: 2003-09-29
Decision date: 2003-12-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Los Angeles, CA, US

Download summary PDF View on FDA.gov ↗

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