AGC-GOLD ELECTROLYTE FOR AGC-MICRO, AGC-GOLD ELECTROLYTE FOR AGC-SPEED, AGC-GOLDBONDER, AGC GLAVANOGOLD— 510(k) K001041

Name: FDA 510(k) clearance K001041
Creator: U.S. Food and Drug Administration
Published: 2000-05-23

Substantially Equivalent

Wieland Edelmetalle GmbH & Co.

FDA 510(k) clearance K001041 for AGC-GOLD ELECTROLYTE FOR AGC-MICRO, AGC-GOLD ELECTROLYTE FOR AGC-SPEED, AGC-GOLDBONDER, AGC GLAVANOGOLD, Substantially Equivalent on 2000-05-23. Applicant: Wieland Edelmetalle GmbH & Co.. Device class: 2.

Clearance details

Applicant: Wieland Edelmetalle GmbH & Co.
Product code: Code EJT
Device class: Class 2
Regulation: 21 CFR 872.3060
Advisory panel: Dental
Date received: 2000-03-31
Decision date: 2000-05-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Pforzheim, DE

Download summary PDF View on FDA.gov ↗

Recent devices under product code EJT

view all

More clearances from Wieland Edelmetalle GmbH & Co.

view all

K020347 — AGC SPEZIALLEGIERUNG2002-04-24
K012839 — AUROPAL, ORDER-NO.: 21012001-12-31
K012841 — DUO PAL 6, ORDER-NO.: 21542001-11-20
K012843 — PORTADUR P 2, MODEL #20312001-11-02
K012826 — BIOPORTA G, MODEL 20522001-11-01

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