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FDA 510(k)

MEISINGER DIAMOND DENTAL BURS

K-Number: K802984 · 1980-12-30

ApplicantSwiss American Metal Craft Corp.
Decision Date1980-12-30
Product CodeDZP
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MEISINGER DIAMOND DENTAL BURS is the device name listed in this FDA 510(k) record. The listed applicant is Swiss American Metal Craft Corp.. It received FDA 510(k) clearance on 1980-12-30 under 510(k) number K802984. 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 MEISINGER DIAMOND DENTAL BURS?

MEISINGER DIAMOND DENTAL BURS is a medical device that received FDA 510(k) clearance on 1980-12-30. The listed applicant is Swiss American Metal Craft Corp.. The 510(k) number is K802984.

When did MEISINGER DIAMOND DENTAL BURS receive FDA 510(k) clearance?

MEISINGER DIAMOND DENTAL BURS received FDA 510(k) clearance on 1980-12-30, under 510(k) number K802984.

Who is the listed applicant for MEISINGER DIAMOND DENTAL BURS?

The FDA 510(k) record lists Swiss American Metal Craft Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEISINGER DIAMOND DENTAL BURS?

The FDA product code for MEISINGER DIAMOND DENTAL BURS 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 Swiss American Metal Craft Corp. 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.

K802989MEISINGER TUNGSTEN CARBIDE & STEEL DT.B.K802988JOTA TUNGSTEN CARBIDE & STEEL DENT. BURSK802987JOTA DIAMOND DENTAL BURS

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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