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FDA 510(k)

BEAVERS' DENTAL DIAMOND INSTRUMENTS

K-Number: K880179 · 1988-03-09

ApplicantBeavers Dental, Div. Sybron Canada, Ltd.
Decision Date1988-03-09
Product CodeDZP
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

BEAVERS' DENTAL DIAMOND INSTRUMENTS 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 1988-03-09 under 510(k) number K880179. The device is classified under product code DZP. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BEAVERS' DENTAL DIAMOND INSTRUMENTS?

BEAVERS' DENTAL DIAMOND INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1988-03-09. The listed applicant is Beavers Dental, Div. Sybron Canada, Ltd.. The 510(k) number is K880179.

When did BEAVERS' DENTAL DIAMOND INSTRUMENTS receive FDA 510(k) clearance?

BEAVERS' DENTAL DIAMOND INSTRUMENTS received FDA 510(k) clearance on 1988-03-09, under 510(k) number K880179.

Who is the listed applicant for BEAVERS' DENTAL DIAMOND INSTRUMENTS?

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 BEAVERS' DENTAL DIAMOND INSTRUMENTS?

The FDA product code for BEAVERS' DENTAL DIAMOND INSTRUMENTS is DZP.

Related Clinical Trials

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.

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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 MODIFIEDK863097CB BUR

Related Devices (Code: DZP)

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 MODIFIEDBeavers Dental, Div. Sybron Canada, Ltd.K943841SOPHOS DENTAL DIAMONDSophos TechnologicK940908DUNHALL/OMNII INTERNATIONAL ROTARY DIAMOND BURSDunhall Pharmaceuticals, Inc.K934981DENTAL DRILLEare Consulting ServiceK923757DENTAL DIAMOND DRILLSAlpha Industrializacao DE Metais Ltda.K913651MANI DIA-BURSThe Lahr Consulting Group, 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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