WIROBOND C— 510(k) K032136

Substantially Equivalent

Bego U.S.A.

FDA 510(k) clearance K032136 for WIROBOND C, Substantially Equivalent on 2003-09-04. Applicant: Bego U.S.A.. Device class: 2.

Clearance details

Applicant: Bego U.S.A.
Product code: Code EJH
Device class: Class 2
Regulation: 21 CFR 872.3710
Advisory panel: Dental
Date received: 2003-07-11
Decision date: 2003-09-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lincoln, RI, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code EJH

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

More clearances from Bego U.S.A.

K033279 — GOLD DENTAL CASTING ALLOYS2004-01-15
K983080 — AUROLLOYD KF1998-10-28
K983082 — BEGOCER G1998-10-28
K983077 — BIO PONTOSTAR1998-10-23
K983078 — BEGOPAL1998-10-23

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