BAR & RIDER, SCREWS, TUBES— 510(k) K790078

Substantially Equivalent

Eurodent, Inc.

FDA 510(k) clearance K790078 for BAR & RIDER, SCREWS, TUBES, Substantially Equivalent on 1979-02-27. Applicant: Eurodent, Inc.. Device class: 1.

Clearance details

Applicant: Eurodent, Inc.
Product code: Code ECG
Device class: Class 1
Regulation: 21 CFR 872.6710
Advisory panel: Dental
Date received: 1979-01-10
Decision date: 1979-02-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code ECG

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K790290 — NEY EQUI-HINGE1979-04-10

More clearances from Eurodent, Inc.

K894058 — ISODENT1989-12-21
K894061 — STUDIO UNO1989-11-21
K894059 — ISOLIGHT1989-09-07
K894060 — ESSE QUATTRO/ESSE UNO1989-09-07

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