TRINDIUM-DENTAL MATERIAL— 510(k) K850084

Name: FDA 510(k) clearance K850084
Creator: U.S. Food and Drug Administration
Published: 1985-07-08

Substantially Equivalent

Trindium Corp. of America

FDA 510(k) clearance K850084 for TRINDIUM-DENTAL MATERIAL, Substantially Equivalent on 1985-07-08. Applicant: Trindium Corp. of America. Device class: 2.

Clearance details

Applicant: Trindium Corp. of America
Product code: Code EJH
Device class: Class 2
Regulation: 21 CFR 872.3710
Advisory panel: Dental
Date received: 1985-01-10
Decision date: 1985-07-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Utica, NY, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code EJH

view all

K123929 — BEGOPAL+2013-03-14
K040180 — CONTINUM V2004-03-04
K040179 — CONTINUM2004-03-03
K033356 — VERASOFT ES2003-12-30
K033045 — DREAM BOND, DREAMCAST CHROME, DREAMCAST V, DREAM FLEXICAST, DREAM LITHECAST2003-12-23

Data sourced from openFDA. This site is unofficial and independent of the FDA.