LUXALLOY 50 (POWDER, TABLETS, PREDOSED CAPSULES)— 510(k) K902249

Name: FDA 510(k) clearance K902249
Creator: U.S. Food and Drug Administration
Published: 1990-07-13

Substantially Equivalent

Degussa AG

FDA 510(k) clearance K902249 for LUXALLOY 50 (POWDER, TABLETS, PREDOSED CAPSULES), Substantially Equivalent on 1990-07-13. Applicant: Degussa AG. Device class: 2.

Clearance details

Applicant: Degussa AG
Product code: Code EJJ
Device class: Class 2
Regulation: 21 CFR 872.3070
Advisory panel: Dental
Date received: 1990-05-18
Decision date: 1990-07-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: West Germany, DE

Download summary PDF View on FDA.gov ↗

Recent devices under product code EJJ

view all

K053114 — SILVERFIL2005-11-15
K051010 — SECURALLOY, SEPTALLOY NG 50 AND SEPTALLOY NG 702005-05-02
K033434 — BESTALOY2003-11-12
K032152 — BENCO ADMIX2003-08-06
K031658 — BENCO SPHERICAL2003-07-29

More clearances from Degussa AG

view all

K953344 — DEGUBOND ULTRA1995-08-25
K931808 — DUCERAGOLD, DUCERATIN1993-11-03
K926347 — DUCERANIUM U1993-05-27
K922790 — DEGUCAST 401992-12-03
K921772 — BIOLOR1992-07-13

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