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FDA 510(k)

F.G. LASER (DENTAL BUR)

K-Number: K901262 · 1990-07-09

ApplicantDiamond Rotary and Carbide Intl.
Decision Date1990-07-09
Product CodeDZP
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

F.G. LASER (DENTAL BUR) is the device name listed in this FDA 510(k) record. The listed applicant is Diamond Rotary and Carbide Intl.. It received FDA 510(k) clearance on 1990-07-09 under 510(k) number K901262. 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 F.G. LASER (DENTAL BUR)?

F.G. LASER (DENTAL BUR) is a medical device that received FDA 510(k) clearance on 1990-07-09. The listed applicant is Diamond Rotary and Carbide Intl.. The 510(k) number is K901262.

When did F.G. LASER (DENTAL BUR) receive FDA 510(k) clearance?

F.G. LASER (DENTAL BUR) received FDA 510(k) clearance on 1990-07-09, under 510(k) number K901262.

Who is the listed applicant for F.G. LASER (DENTAL BUR)?

The FDA 510(k) record lists Diamond Rotary and Carbide Intl. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for F.G. LASER (DENTAL BUR)?

The FDA product code for F.G. LASER (DENTAL BUR) 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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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