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FDA 510(k)

DENTAL DIAMOND DRILLS

K-Number: K923757 · 1993-03-16

Decision Date1993-03-16
Product CodeDZP
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DENTAL DIAMOND DRILLS is the device name listed in this FDA 510(k) record. The listed applicant is Alpha Industrializacao DE Metais Ltda.. It received FDA 510(k) clearance on 1993-03-16 under 510(k) number K923757. 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 DENTAL DIAMOND DRILLS?

DENTAL DIAMOND DRILLS is a medical device that received FDA 510(k) clearance on 1993-03-16. The listed applicant is Alpha Industrializacao DE Metais Ltda.. The 510(k) number is K923757.

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

DENTAL DIAMOND DRILLS received FDA 510(k) clearance on 1993-03-16, under 510(k) number K923757.

Who is the listed applicant for DENTAL DIAMOND DRILLS?

The FDA 510(k) record lists Alpha Industrializacao DE Metais Ltda. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DENTAL DIAMOND DRILLS?

The FDA product code for DENTAL DIAMOND DRILLS 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.

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.

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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