F.G. LASER (DENTAL BUR)— 510(k) K901262

Name: FDA 510(k) clearance K901262
Creator: U.S. Food and Drug Administration
Published: 1990-07-09

Substantially Equivalent

Diamond Rotary and Carbide Intl.

FDA 510(k) clearance K901262 for F.G. LASER (DENTAL BUR), Substantially Equivalent on 1990-07-09. Applicant: Diamond Rotary and Carbide Intl.. Device class: 1.

Clearance details

Applicant: Diamond Rotary and Carbide Intl.
Product code: Code DZP
Device class: Class 1
Regulation: 21 CFR 872.4535
Advisory panel: Dental
Date received: 1990-03-16
Decision date: 1990-07-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Canada R3c 4e5, CA

Download summary PDF View on FDA.gov ↗

Recent devices under product code DZP

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K120037 — BLUWHITE DIAMOND DENTAL BURS MODIFIED2012-04-20
K943841 — SOPHOS DENTAL DIAMOND1994-09-16
K940908 — DUNHALL/OMNII INTERNATIONAL ROTARY DIAMOND BURS1994-08-29
K934981 — DENTAL DRILL1994-02-03
K923757 — DENTAL DIAMOND DRILLS1993-03-16

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