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FDA 510(k)

3D DENTAL DIAMOND ROTARY INSTRUMENTS

K-Number: K893844 · 1989-08-11

ApplicantLustgarten Multi-Tech International, Inc.
Decision Date1989-08-11
Product CodeDZP
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

3D DENTAL DIAMOND ROTARY INSTRUMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Lustgarten Multi-Tech International, Inc.. It received FDA 510(k) clearance on 1989-08-11 under 510(k) number K893844. 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 3D DENTAL DIAMOND ROTARY INSTRUMENTS?

3D DENTAL DIAMOND ROTARY INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1989-08-11. The listed applicant is Lustgarten Multi-Tech International, Inc.. The 510(k) number is K893844.

When did 3D DENTAL DIAMOND ROTARY INSTRUMENTS receive FDA 510(k) clearance?

3D DENTAL DIAMOND ROTARY INSTRUMENTS received FDA 510(k) clearance on 1989-08-11, under 510(k) number K893844.

Who is the listed applicant for 3D DENTAL DIAMOND ROTARY INSTRUMENTS?

The FDA 510(k) record lists Lustgarten Multi-Tech International, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 3D DENTAL DIAMOND ROTARY INSTRUMENTS?

The FDA product code for 3D DENTAL DIAMOND ROTARY 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 Lustgarten Multi-Tech International, Inc. 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.

K895085WALKLITE PROTABLE RE-CHARGEABLE CURING LIGHTK874458PRIME PLUS-POLYACRYLIC ACID BOND CONDITIONER

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

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

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