BEAVERS' DENTAL DIAMOND INSTRUMENTS— 510(k) K880179

Name: FDA 510(k) clearance K880179
Creator: U.S. Food and Drug Administration
Published: 1988-03-09

Substantially Equivalent

Beavers Dental, Div. Sybron Canada, Ltd.

FDA 510(k) clearance K880179 for BEAVERS' DENTAL DIAMOND INSTRUMENTS, Substantially Equivalent on 1988-03-09. Applicant: Beavers Dental, Div. Sybron Canada, Ltd.. Device class: 1.

Clearance details

Applicant: Beavers Dental, Div. Sybron Canada, Ltd.
Product code: Code DZP
Device class: Class 1
Regulation: 21 CFR 872.4535
Advisory panel: Dental
Date received: 1988-01-13
Decision date: 1988-03-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

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