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FDA 510(k)

HIGH SPEED DENTAL DRILL/HANDPIECE

K-Number: K925739 · 1993-07-22

Decision Date1993-07-22
Product CodeEFB
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

HIGH SPEED DENTAL DRILL/HANDPIECE is the device name listed in this FDA 510(k) record. The listed applicant is Feather Touch, Inc.. It received FDA 510(k) clearance on 1993-07-22 under 510(k) number K925739. The device is classified under product code EFB. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HIGH SPEED DENTAL DRILL/HANDPIECE?

HIGH SPEED DENTAL DRILL/HANDPIECE is a medical device that received FDA 510(k) clearance on 1993-07-22. The listed applicant is Feather Touch, Inc.. The 510(k) number is K925739.

When did HIGH SPEED DENTAL DRILL/HANDPIECE receive FDA 510(k) clearance?

HIGH SPEED DENTAL DRILL/HANDPIECE received FDA 510(k) clearance on 1993-07-22, under 510(k) number K925739.

Who is the listed applicant for HIGH SPEED DENTAL DRILL/HANDPIECE?

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

What is the FDA product code for HIGH SPEED DENTAL DRILL/HANDPIECE?

The FDA product code for HIGH SPEED DENTAL DRILL/HANDPIECE is EFB.

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: EFB)

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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