FIBIOCORE— 510(k) K020431

Substantially Equivalent

Est. Anthogyr

FDA 510(k) clearance K020431 for FIBIOCORE, Substantially Equivalent on 2002-07-03. Applicant: Est. Anthogyr. Device class: 1.

Clearance details

Applicant: Est. Anthogyr
Product code: Code ELR
Device class: Class 1
Regulation: 21 CFR 872.3810
Advisory panel: Dental
Date received: 2002-02-08
Decision date: 2002-07-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sallanches, FR

Download summary PDF View on FDA.gov ↗

Recent devices under product code ELR

More clearances from Est. Anthogyr

K070084 — MONTBLANC IMPLANTOLOGY CONTRA ANGLE CONTROL2007-03-08
K060317 — ANTHOGYR CONTRA ANGLES AND HANDPIECES2006-04-28

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