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FDA 510(k)

ANEST-EZE DENTAL DRILL RA#2

K-Number: K896149 · 1990-01-19

Decision Date1990-01-19
Product CodeDZA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ANEST-EZE DENTAL DRILL RA#2 is the device name listed in this FDA 510(k) record. The listed applicant is Signature One Products, Inc.. It received FDA 510(k) clearance on 1990-01-19 under 510(k) number K896149. The device is classified under product code DZA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANEST-EZE DENTAL DRILL RA#2?

ANEST-EZE DENTAL DRILL RA#2 is a medical device that received FDA 510(k) clearance on 1990-01-19. The listed applicant is Signature One Products, Inc.. The 510(k) number is K896149.

When did ANEST-EZE DENTAL DRILL RA#2 receive FDA 510(k) clearance?

ANEST-EZE DENTAL DRILL RA#2 received FDA 510(k) clearance on 1990-01-19, under 510(k) number K896149.

Who is the listed applicant for ANEST-EZE DENTAL DRILL RA#2?

The FDA 510(k) record lists Signature One Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ANEST-EZE DENTAL DRILL RA#2?

The FDA product code for ANEST-EZE DENTAL DRILL RA#2 is DZA.

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: DZA)

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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