Cleared Traditional

BEAVERS' DENTAL DIAMOND INSTRUMENTS

K880179 · Beavers Dental, Div. Sybron Canada, Ltd. · Dental

Mar 1988

Decision

56d

Days

Class 1

Risk

About This 510(k) Submission

K880179 is an FDA 510(k) clearance for the BEAVERS' DENTAL DIAMOND INSTRUMENTS, a Instrument, Diamond, Dental (Class I — General Controls, product code DZP), submitted by Beavers Dental, Div. Sybron Canada, Ltd. (Washington, US). The FDA issued a Cleared decision on March 9, 1988, 56 days after receiving the submission on January 13, 1988. This device falls under the Dental review panel. Regulated under 21 CFR 872.4535.

Submission Details

510(k) Number	K880179 FDA.gov
FDA Decision	Cleared SESE
Date Received	January 13, 1988
Decision Date	March 09, 1988
Days to Decision	56 days
Submission Type	Traditional
Review Panel	Dental (DE)
Summary	—