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FDA 510(k)

CB BUR

K-Number: K863097 · 1986-08-26

ApplicantBeavers Dental, Div. Sybron Canada, Ltd.
Decision Date1986-08-26
Product CodeEJL
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CB BUR is the device name listed in this FDA 510(k) record. The listed applicant is Beavers Dental, Div. Sybron Canada, Ltd.. It received FDA 510(k) clearance on 1986-08-26 under 510(k) number K863097. The device is classified under product code EJL. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CB BUR?

CB BUR is a medical device that received FDA 510(k) clearance on 1986-08-26. The listed applicant is Beavers Dental, Div. Sybron Canada, Ltd.. The 510(k) number is K863097.

When did CB BUR receive FDA 510(k) clearance?

CB BUR received FDA 510(k) clearance on 1986-08-26, under 510(k) number K863097.

Who is the listed applicant for CB BUR?

The FDA 510(k) record lists Beavers Dental, Div. Sybron Canada, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CB BUR?

The FDA product code for CB BUR is EJL.

Other records listing Beavers Dental, Div. Sybron Canada, Ltd. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K120037BLUWHITE DIAMOND DENTAL BURS MODIFIEDK880179BEAVERS' DENTAL DIAMOND INSTRUMENTS

Related Devices (Code: EJL)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K080687SMARTBURSS.S. White Burs, Inc.K071352CERADRILLGebr. Brasseler GmbH & Co. KGK061383BTI STERILE DENTAL DRILLS KIT, BTI ABUTMENTS AND CAPSB.T.I. Biotechnology Institute, Sl.K943273TRI HAWK BUR, FG BURTri Hawk Corp.K926205MONOSTERYLUtensili Super AbrasiviK923883DENTAL OR SURGICAL BURStratum Dental Technologies, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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